|
ENST00000412971.6:c.1135T>G
|
ENSP00000410263.2:p.Ser379Ala
|
|
|
ENST00000435155.2:c.1552T>G
|
ENSP00000403655.2:p.Ser518Ala
|
|
|
ENST00000467459.6:c.*381T>G
|
ENSP00000435889.2:n.*381T>G
|
|
|
ENST00000483127.2:c.1537T>G
|
ENSP00000436469.2:p.Ser513Ala
|
|
|
ENST00000485271.6:c.*262T>G
|
ENSP00000431264.2:n.*262T>G
|
|
|
ENST00000529892.6:c.1372T>G
|
ENSP00000432528.2:p.Ser458Ala
|
|
|
ENST00000533178.6:c.*848T>G
|
ENSP00000436430.2:n.*848T>G
|
|
|
ENST00000672314.2:c.1519T>G
|
ENSP00000500828.2:p.Ser507Ala
|
|
|
ENST00000710952.2:c.1603T>G
MANE Plus Clinical
|
ENSP00000518552.2:p.Ser535Ala
|
|
|
ENST00000672818.3:c.1594T>G
|
ENSP00000500891.1:p.Ser532Ala
|
|
|
ENST00000456914.7:c.1519T>G
MANE Select
|
ENSP00000407590.2:p.Ser507Ala
|
|
|
ENST00000671898.1:c.*262T>G
|
ENSP00000499896.1:n.*262T>G
|
|
|
ENST00000672011.1:c.*848T>G
|
ENSP00000500418.1:n.*848T>G
|
|
|
ENST00000672818.2:c.1594T>G
|
ENSP00000500891.1:p.Ser532Ala
|
|
|
ENST00000354383.10:c.1522T>G
|
ENSP00000346354.6:p.Ser508Ala
|
|
|
ENST00000355498.6:c.1519T>G
|
ENSP00000347685.2:p.Ser507Ala
|
|
|
ENST00000372098.7:c.1594T>G
|
ENSP00000361170.3:p.Ser532Ala
|
|
|
ENST00000372104.5:c.1519T>G
|
ENSP00000361176.1:p.Ser507Ala
|
|
|
ENST00000372110.7:c.1564T>G
|
ENSP00000361182.3:p.Ser522Ala
|
|
|
ENST00000372115.7:c.1561T>G
|
ENSP00000361187.3:p.Ser521Ala
|
|
|
ENST00000448481.5:c.1552T>G
|
ENSP00000409718.1:p.Ser518Ala
|
|
|
ENST00000450313.5:c.1603T>G
|
ENSP00000408176.1:p.Ser535Ala
|
|
|
ENST00000456914.6:c.1519T>G
|
ENSP00000407590.2:p.Ser507Ala
|
|
|
ENST00000467459.5:c.936T>G
|
ENSP00000435889.1:n.936T>G
|
|
|
ENST00000475516.5:c.*1332T>G
|
ENSP00000433843.1:n.*1332T>G
|
|
|
ENST00000481571.5:c.*1332T>G
|
ENSP00000436597.1:n.*1332T>G
|
|
|
ENST00000482094.5:n.840T>G
|
|
|
|
ENST00000485271.5:c.396T>G
|
|
|
|
ENST00000488731.6:c.604T>G
|
ENSP00000432330.1:p.Ser202Ala
|
|
|
ENST00000528013.6:c.1561T>G
|
ENSP00000433130.2:p.Ser521Ala
|
|
|
ENST00000529892.5:c.594T>G
|
|
|
|
ENST00000529984.5:c.604T>G
|
ENSP00000437093.1:p.Ser202Ala
|
|
|
ENST00000531105.5:c.*11T>G
|
ENSP00000431292.1:n.*11T>G
|
|
|
ENST00000533178.5:c.1148T>G
|
ENSP00000436430.1:n.1148T>G
|
|
|
NM_001048171.1:c.1561T>G
|
NP_001041636.1:p.Ser521Ala
|
|
|
NM_001048172.1:c.1522T>G
|
NP_001041637.1:p.Ser508Ala
|
|
|
NM_001048173.1:c.1519T>G
|
NP_001041638.1:p.Ser507Ala
|
|
|
NM_001048174.1:c.1519T>G
|
NP_001041639.1:p.Ser507Ala
|
|
|
NM_001128425.1:c.1603T>G , LRG_220t1:c.1603T>G
|
NP_001121897.1:p.Ser535Ala
|
|
|
NM_001293190.1:c.1564T>G
|
NP_001280119.1:p.Ser522Ala
|
|
|
NM_001293191.1:c.1552T>G
|
NP_001280120.1:p.Ser518Ala
|
|
|
NM_001293192.1:c.1243T>G
|
NP_001280121.1:p.Ser415Ala
|
|
|
NM_001293195.1:c.1519T>G
|
NP_001280124.1:p.Ser507Ala
|
|
|
NM_001293196.1:c.1243T>G
|
NP_001280125.1:p.Ser415Ala
|
|
|
NM_012222.2:c.1594T>G
|
NP_036354.1:p.Ser532Ala
|
|
|
XM_011541497.1:c.1579T>G
|
XP_011539799.1:p.Ser527Ala
|
|
|
XM_011541498.1:c.1561T>G
|
XP_011539800.1:p.Ser521Ala
|
|
|
XM_011541499.1:c.1561T>G
|
XP_011539801.1:p.Ser521Ala
|
|
|
XM_011541500.1:c.1561T>G
|
XP_011539802.1:p.Ser521Ala
|
|
|
XM_011541501.1:c.1561T>G
|
XP_011539803.1:p.Ser521Ala
|
|
|
XM_011541502.1:c.1561T>G
|
XP_011539804.1:p.Ser521Ala
|
|
|
XM_011541503.1:c.1561T>G
|
XP_011539805.1:p.Ser521Ala
|
|
|
XM_011541504.1:c.1552T>G
|
XP_011539806.1:p.Ser518Ala
|
|
|
XM_011541505.1:c.1141T>G
|
XP_011539807.1:p.Ser381Ala
|
|
|
XM_011541506.1:c.1141T>G
|
XP_011539808.1:p.Ser381Ala
|
|
|
XM_011541507.1:c.1132T>G
|
XP_011539809.1:p.Ser378Ala
|
|
|
XM_011541508.1:c.1147T>G
|
XP_011539810.1:p.Ser383Ala
|
|
|
XR_946658.1:n.1830T>G
|
|
|
|
NM_001350650.1:c.1174T>G
|
NP_001337579.1:p.Ser392Ala
|
|
|
NM_001350651.1:c.1174T>G
|
NP_001337580.1:p.Ser392Ala
|
|
|
NR_146882.1:n.1957T>G
|
|
|
|
NR_146883.1:n.1771T>G
|
|
|
|
XM_011541497.3:c.1579T>G
|
XP_011539799.1:p.Ser527Ala
|
|
|
XM_011541500.3:c.1561T>G
|
XP_011539802.1:p.Ser521Ala
|
|
|
XM_011541501.2:c.1561T>G
|
XP_011539803.1:p.Ser521Ala
|
|
|
XM_011541502.2:c.1561T>G
|
XP_011539804.1:p.Ser521Ala
|
|
|
XM_011541503.2:c.1561T>G
|
XP_011539805.1:p.Ser521Ala
|
|
|
XM_011541504.2:c.1552T>G
|
XP_011539806.1:p.Ser518Ala
|
|
|
XM_011541505.2:c.1141T>G
|
XP_011539807.1:p.Ser381Ala
|
|
|
XM_011541506.2:c.1141T>G
|
XP_011539808.1:p.Ser381Ala
|
|
|
XM_017001331.1:c.1561T>G
|
XP_016856820.1:p.Ser521Ala
|
|
|
XM_017001332.1:c.1561T>G
|
XP_016856821.1:p.Ser521Ala
|
|
|
XM_017001333.1:c.1561T>G
|
XP_016856822.1:p.Ser521Ala
|
|
|
XM_017001334.1:c.1522T>G
|
XP_016856823.1:p.Ser508Ala
|
|
|
XM_017001335.1:c.1243T>G
|
XP_016856824.1:p.Ser415Ala
|
|
|
XM_017001336.1:c.1174T>G
|
XP_016856825.1:p.Ser392Ala
|
|
|
XM_017001337.1:c.1174T>G
|
XP_016856826.1:p.Ser392Ala
|
|
|
XM_024447244.1:c.1174T>G
|
XP_024303012.1:p.Ser392Ala
|
|
|
XM_024447245.1:c.1174T>G
|
XP_024303013.1:p.Ser392Ala
|
|
|
XM_024447248.1:c.1132T>G
|
XP_024303016.1:p.Ser378Ala
|
|
|
XM_024447249.1:c.1003T>G
|
XP_024303017.1:p.Ser335Ala
|
|
|
XM_024447250.1:c.1003T>G
|
XP_024303018.1:p.Ser335Ala
|
|
|
XM_024447251.1:c.1003T>G
|
XP_024303019.1:p.Ser335Ala
|
|
|
XR_001737190.1:n.1744T>G
|
|
|
|
XR_001737192.1:n.1556T>G
|
|
|
|
XR_002956643.1:n.1736T>G
|
|
|
|
XR_002956644.1:n.2271T>G
|
|
|
|
XR_946658.2:n.1844T>G
|
|
|
|
NM_001048171.2:c.1519T>G
|
NP_001041636.2:p.Ser507Ala
|
|
|
NM_001128425.2:c.1603T>G
MANE Plus Clinical
|
NP_001121897.1:p.Ser535Ala
|
|
|
NM_001048172.2:c.1522T>G
|
NP_001041637.1:p.Ser508Ala
|
|
|
NM_001048173.2:c.1519T>G
|
NP_001041638.1:p.Ser507Ala
|
|
|
NM_001048174.2:c.1519T>G
MANE Select
|
NP_001041639.1:p.Ser507Ala
|
|
|
NM_001293190.2:c.1564T>G
|
NP_001280119.1:p.Ser522Ala
|
|
|
NM_001293191.2:c.1552T>G
|
NP_001280120.1:p.Ser518Ala
|
|
|
NM_001293192.2:c.1243T>G
|
NP_001280121.1:p.Ser415Ala
|
|
|
NM_001293195.2:c.1519T>G
|
NP_001280124.1:p.Ser507Ala
|
|
|
NM_001293196.2:c.1243T>G
|
NP_001280125.1:p.Ser415Ala
|
|
|
NM_001350650.2:c.1174T>G
|
NP_001337579.1:p.Ser392Ala
|
|
|
NM_001350651.2:c.1174T>G
|
NP_001337580.1:p.Ser392Ala
|
|
|
NM_012222.3:c.1594T>G
|
NP_036354.1:p.Ser532Ala
|
|
|
NR_146882.2:n.1927T>G
|
|
|
|
NR_146883.2:n.1776T>G
|
|
|
