ENST00000405392.6:c.2750G>C
|
ENSP00000384484.2:p.Ser917Thr
|
|
ENST00000679454.1:c.2747G>C
MANE Select
|
ENSP00000505261.1:p.Ser916Thr
|
|
ENST00000260600.9:c.2747G>C
|
ENSP00000260600.5:p.Ser916Thr
|
|
ENST00000405392.5:c.2750G>C
|
ENSP00000384484.2:p.Ser917Thr
|
|
ENST00000485887.1:n.19G>C
|
|
|
ENST00000606682.5:c.1688G>C
|
ENSP00000475652.1:p.Ser563Thr
|
|
NM_004036.3:c.2747G>C
|
NP_004027.2:p.Ser916Thr
|
|
XM_005264104.1:c.2750G>C
|
XP_005264161.1:p.Ser917Thr
|
|
XM_005264105.1:c.2747G>C
|
XP_005264162.1:p.Ser916Thr
|
|
XM_006711925.1:c.2816G>C
|
XP_006711988.1:p.Ser939Thr
|
|
XM_011532489.1:c.2873G>C
|
XP_011530791.1:p.Ser958Thr
|
|
XM_011532490.1:c.2870G>C
|
XP_011530792.1:p.Ser957Thr
|
|
XM_011532491.1:c.2807G>C
|
XP_011530793.1:p.Ser936Thr
|
|
XM_011532492.1:c.2873G>C
|
XP_011530794.1:p.Ser958Thr
|
|
XM_011532493.1:c.2735G>C
|
XP_011530795.1:p.Ser912Thr
|
|
XM_011532494.1:c.2675G>C
|
XP_011530796.1:p.Ser892Thr
|
|
XM_011532495.1:c.2207G>C
|
XP_011530797.1:p.Ser736Thr
|
|
XM_011532496.1:c.2150G>C
|
XP_011530798.1:p.Ser717Thr
|
|
NM_001320613.1:c.2750G>C
|
NP_001307542.1:p.Ser917Thr
|
|
NM_004036.4:c.2747G>C
|
NP_004027.2:p.Ser916Thr
|
|
XM_011532492.2:c.2873G>C
|
XP_011530794.1:p.Ser958Thr
|
|
XM_017003186.1:c.2813G>C
|
XP_016858675.1:p.Ser938Thr
|
|
XM_017003187.1:c.2804G>C
|
XP_016858676.1:p.Ser935Thr
|
|
XM_017003188.1:c.2870G>C
|
XP_016858677.1:p.Ser957Thr
|
|
XM_017003189.1:c.2732G>C
|
XP_016858678.1:p.Ser911Thr
|
|
XM_017003190.1:c.2609G>C
|
XP_016858679.1:p.Ser870Thr
|
|
XM_017003191.1:c.2237G>C
|
XP_016858680.1:p.Ser746Thr
|
|
XM_017003192.1:c.2027G>C
|
XP_016858681.1:p.Ser676Thr
|
|
XM_017003193.1:c.2024G>C
|
XP_016858682.1:p.Ser675Thr
|
|
NM_001320613.2:c.2750G>C
|
NP_001307542.1:p.Ser917Thr
|
|
NM_001377128.1:c.2813G>C
|
NP_001364057.1:p.Ser938Thr
|
|
NM_001377129.1:c.2609G>C
|
NP_001364058.1:p.Ser870Thr
|
|
NM_001377130.1:c.2332-715G>C
|
NP_001364059.1:n.2332-715G>C
|
|
NM_001377131.1:c.2024G>C
|
NP_001364060.1:p.Ser675Thr
|
|
NM_001377132.1:c.2747G>C
|
NP_001364061.1:p.Ser916Thr
|
|
NM_004036.5:c.2747G>C
MANE Select
|
NP_004027.2:p.Ser916Thr
|
|