|
ENST00000412971.6:c.142A>G
|
ENSP00000410263.2:p.Thr48Ala
|
|
|
ENST00000435155.2:c.559A>G
|
ENSP00000403655.2:p.Thr187Ala
|
|
|
ENST00000467459.6:c.526A>G
|
ENSP00000435889.2:p.Thr176Ala
|
|
|
ENST00000483127.2:c.544A>G
|
ENSP00000436469.2:p.Thr182Ala
|
|
|
ENST00000485271.6:c.526A>G
|
ENSP00000431264.2:p.Thr176Ala
|
|
|
ENST00000529892.6:c.568A>G
|
ENSP00000432528.2:p.Thr190Ala
|
|
|
ENST00000533178.6:c.149A>G
|
ENSP00000436430.2:p.Tyr50Cys
|
|
|
ENST00000672314.2:c.526A>G
|
ENSP00000500828.2:p.Thr176Ala
|
|
|
ENST00000674679.2:c.*438A>G
|
ENSP00000501623.2:n.*438A>G
|
|
|
ENST00000710952.2:c.610A>G
MANE Plus Clinical
|
ENSP00000518552.2:p.Thr204Ala
|
|
|
ENST00000672818.3:c.601A>G
|
ENSP00000500891.1:p.Thr201Ala
|
|
|
ENST00000450313.6:c.536A>G
|
ENSP00000408176.2:p.Tyr179Cys
|
|
|
ENST00000456914.7:c.526A>G
MANE Select
|
ENSP00000407590.2:p.Thr176Ala
|
|
|
ENST00000461495.6:c.*265A>G
|
ENSP00000437166.1:n.*265A>G
|
|
|
ENST00000671856.1:n.472A>G
|
|
|
|
ENST00000671898.1:c.1114A>G
|
ENSP00000499896.1:p.Thr372Ala
|
|
|
ENST00000672011.1:c.494A>G
|
ENSP00000500418.1:p.Tyr165Cys
|
|
|
ENST00000672314.1:c.526A>G
|
ENSP00000500828.1:p.Thr176Ala
|
|
|
ENST00000672593.1:c.*414A>G
|
ENSP00000500455.1:n.*414A>G
|
|
|
ENST00000672764.1:c.485A>G
|
ENSP00000500886.1:p.Tyr162Cys
|
|
|
ENST00000672818.2:c.601A>G
|
ENSP00000500891.1:p.Thr201Ala
|
|
|
ENST00000673134.1:c.*223A>G
|
ENSP00000500526.1:n.*223A>G
|
|
|
ENST00000674679.1:c.554A>G
|
ENSP00000501623.1:n.554A>G
|
|
|
ENST00000354383.10:c.529A>G
|
ENSP00000346354.6:p.Thr177Ala
|
|
|
ENST00000355498.6:c.526A>G
|
ENSP00000347685.2:p.Thr176Ala
|
|
|
ENST00000372098.7:c.601A>G
|
ENSP00000361170.3:p.Thr201Ala
|
|
|
ENST00000372104.5:c.526A>G
|
ENSP00000361176.1:p.Thr176Ala
|
|
|
ENST00000372110.7:c.571A>G
|
ENSP00000361182.3:p.Thr191Ala
|
|
|
ENST00000372115.7:c.568A>G
|
ENSP00000361187.3:p.Thr190Ala
|
|
|
ENST00000412971.5:c.142A>G
|
ENSP00000410263.1:p.Thr48Ala
|
|
|
ENST00000435155.1:c.559A>G
|
ENSP00000403655.1:p.Thr187Ala
|
|
|
ENST00000448481.5:c.559A>G
|
ENSP00000409718.1:p.Thr187Ala
|
|
|
ENST00000450313.5:c.610A>G
|
ENSP00000408176.1:p.Thr204Ala
|
|
|
ENST00000456914.6:c.526A>G
|
ENSP00000407590.2:p.Thr176Ala
|
|
|
ENST00000461495.5:c.*265A>G
|
ENSP00000437166.1:n.*265A>G
|
|
|
ENST00000462388.5:n.217A>G
|
|
|
|
ENST00000467940.5:c.*449A>G
|
ENSP00000436478.1:n.*449A>G
|
|
|
ENST00000470256.5:c.413A>G
|
ENSP00000434985.1:p.Tyr138Cys
|
|
|
ENST00000475516.5:c.*339A>G
|
ENSP00000433843.1:n.*339A>G
|
|
|
ENST00000478796.5:n.513A>G
|
|
|
|
ENST00000479746.6:n.884A>G
|
|
|
|
ENST00000481571.5:c.*339A>G
|
ENSP00000436597.1:n.*339A>G
|
|
|
ENST00000483642.5:n.1041A>G
|
|
|
|
ENST00000488731.6:c.187+109A>G
|
ENSP00000432330.1:n.187+109A>G
|
|
|
ENST00000492494.5:n.923A>G
|
|
|
|
ENST00000525160.5:c.*177A>G
|
ENSP00000431568.1:n.*177A>G
|
|
|
ENST00000528013.6:c.568A>G
|
ENSP00000433130.2:p.Thr190Ala
|
|
|
ENST00000529984.5:c.187+109A>G
|
ENSP00000437093.1:n.187+109A>G
|
|
|
ENST00000531105.5:c.115+1737A>G
|
ENSP00000431292.1:n.115+1737A>G
|
|
|
ENST00000533178.5:c.155A>G
|
ENSP00000436430.1:p.Tyr52Cys
|
|
|
NM_001048171.1:c.568A>G
|
NP_001041636.1:p.Thr190Ala
|
|
|
NM_001048172.1:c.529A>G
|
NP_001041637.1:p.Thr177Ala
|
|
|
NM_001048173.1:c.526A>G
|
NP_001041638.1:p.Thr176Ala
|
|
|
NM_001048174.1:c.526A>G
|
NP_001041639.1:p.Thr176Ala
|
|
|
NM_001128425.1:c.610A>G , LRG_220t1:c.610A>G
|
NP_001121897.1:p.Thr204Ala
|
|
|
NM_001293190.1:c.571A>G
|
NP_001280119.1:p.Thr191Ala
|
|
|
NM_001293191.1:c.559A>G
|
NP_001280120.1:p.Thr187Ala
|
|
|
NM_001293192.1:c.250A>G
|
NP_001280121.1:p.Thr84Ala
|
|
|
NM_001293195.1:c.526A>G
|
NP_001280124.1:p.Thr176Ala
|
|
|
NM_001293196.1:c.250A>G
|
NP_001280125.1:p.Thr84Ala
|
|
|
NM_012222.2:c.601A>G
|
NP_036354.1:p.Thr201Ala
|
|
|
XM_011541497.1:c.586A>G
|
XP_011539799.1:p.Thr196Ala
|
|
|
XM_011541498.1:c.568A>G
|
XP_011539800.1:p.Thr190Ala
|
|
|
XM_011541499.1:c.568A>G
|
XP_011539801.1:p.Thr190Ala
|
|
|
XM_011541500.1:c.568A>G
|
XP_011539802.1:p.Thr190Ala
|
|
|
XM_011541501.1:c.568A>G
|
XP_011539803.1:p.Thr190Ala
|
|
|
XM_011541502.1:c.568A>G
|
XP_011539804.1:p.Thr190Ala
|
|
|
XM_011541503.1:c.568A>G
|
XP_011539805.1:p.Thr190Ala
|
|
|
XM_011541504.1:c.559A>G
|
XP_011539806.1:p.Thr187Ala
|
|
|
XM_011541505.1:c.148A>G
|
XP_011539807.1:p.Thr50Ala
|
|
|
XM_011541506.1:c.148A>G
|
XP_011539808.1:p.Thr50Ala
|
|
|
XM_011541507.1:c.139A>G
|
XP_011539809.1:p.Thr47Ala
|
|
|
XM_011541508.1:c.154A>G
|
XP_011539810.1:p.Thr52Ala
|
|
|
XR_946658.1:n.657A>G
|
|
|
|
NM_001350650.1:c.181A>G
|
NP_001337579.1:p.Thr61Ala
|
|
|
NM_001350651.1:c.181A>G
|
NP_001337580.1:p.Thr61Ala
|
|
|
NR_146882.1:n.784A>G
|
|
|
|
NR_146883.1:n.598A>G
|
|
|
|
XM_011541497.3:c.586A>G
|
XP_011539799.1:p.Thr196Ala
|
|
|
XM_011541500.3:c.568A>G
|
XP_011539802.1:p.Thr190Ala
|
|
|
XM_011541501.2:c.568A>G
|
XP_011539803.1:p.Thr190Ala
|
|
|
XM_011541502.2:c.568A>G
|
XP_011539804.1:p.Thr190Ala
|
|
|
XM_011541503.2:c.568A>G
|
XP_011539805.1:p.Thr190Ala
|
|
|
XM_011541504.2:c.559A>G
|
XP_011539806.1:p.Thr187Ala
|
|
|
XM_011541505.2:c.148A>G
|
XP_011539807.1:p.Thr50Ala
|
|
|
XM_011541506.2:c.148A>G
|
XP_011539808.1:p.Thr50Ala
|
|
|
XM_017001331.1:c.568A>G
|
XP_016856820.1:p.Thr190Ala
|
|
|
XM_017001332.1:c.568A>G
|
XP_016856821.1:p.Thr190Ala
|
|
|
XM_017001333.1:c.568A>G
|
XP_016856822.1:p.Thr190Ala
|
|
|
XM_017001334.1:c.529A>G
|
XP_016856823.1:p.Thr177Ala
|
|
|
XM_017001335.1:c.250A>G
|
XP_016856824.1:p.Thr84Ala
|
|
|
XM_017001336.1:c.181A>G
|
XP_016856825.1:p.Thr61Ala
|
|
|
XM_017001337.1:c.181A>G
|
XP_016856826.1:p.Thr61Ala
|
|
|
XM_024447244.1:c.181A>G
|
XP_024303012.1:p.Thr61Ala
|
|
|
XM_024447245.1:c.181A>G
|
XP_024303013.1:p.Thr61Ala
|
|
|
XM_024447248.1:c.139A>G
|
XP_024303016.1:p.Thr47Ala
|
|
|
XM_024447249.1:c.10A>G
|
XP_024303017.1:p.Thr4Ala
|
|
|
XM_024447250.1:c.10A>G
|
XP_024303018.1:p.Thr4Ala
|
|
|
XM_024447251.1:c.10A>G
|
XP_024303019.1:p.Thr4Ala
|
|
|
XR_001737190.1:n.571A>G
|
|
|
|
XR_001737192.1:n.383A>G
|
|
|
|
XR_002956643.1:n.563A>G
|
|
|
|
XR_002956644.1:n.1098A>G
|
|
|
|
XR_946658.2:n.671A>G
|
|
|
|
NM_001048171.2:c.526A>G
|
NP_001041636.2:p.Thr176Ala
|
|
|
NM_001128425.2:c.610A>G
MANE Plus Clinical
|
NP_001121897.1:p.Thr204Ala
|
|
|
NM_001048172.2:c.529A>G
|
NP_001041637.1:p.Thr177Ala
|
|
|
NM_001048173.2:c.526A>G
|
NP_001041638.1:p.Thr176Ala
|
|
|
NM_001048174.2:c.526A>G
MANE Select
|
NP_001041639.1:p.Thr176Ala
|
|
|
NM_001293190.2:c.571A>G
|
NP_001280119.1:p.Thr191Ala
|
|
|
NM_001293191.2:c.559A>G
|
NP_001280120.1:p.Thr187Ala
|
|
|
NM_001293192.2:c.250A>G
|
NP_001280121.1:p.Thr84Ala
|
|
|
NM_001293195.2:c.526A>G
|
NP_001280124.1:p.Thr176Ala
|
|
|
NM_001293196.2:c.250A>G
|
NP_001280125.1:p.Thr84Ala
|
|
|
NM_001350650.2:c.181A>G
|
NP_001337579.1:p.Thr61Ala
|
|
|
NM_001350651.2:c.181A>G
|
NP_001337580.1:p.Thr61Ala
|
|
|
NM_012222.3:c.601A>G
|
NP_036354.1:p.Thr201Ala
|
|
|
NR_146882.2:n.754A>G
|
|
|
|
NR_146883.2:n.603A>G
|
|
|
