ENST00000264380.9:c.3407C>G
MANE Select
|
ENSP00000264380.4:p.Thr1136Ser
|
|
ENST00000264380.8:c.3407C>G
|
ENSP00000264380.4:p.Thr1136Ser
|
|
ENST00000452564.1:c.3239C>G
|
ENSP00000405736.1:p.Thr1080Ser
|
|
NM_015040.3:c.3407C>G
|
NP_055855.2:p.Thr1136Ser
|
|
XM_011510778.1:c.3443C>G
|
XP_011509080.1:p.Thr1148Ser
|
|
XM_011510779.1:c.3443C>G
|
XP_011509081.1:p.Thr1148Ser
|
|
XM_011510780.1:c.3440C>G
|
XP_011509082.1:p.Thr1147Ser
|
|
XM_011510781.1:c.3425C>G
|
XP_011509083.1:p.Thr1142Ser
|
|
XM_011510782.1:c.3443C>G
|
XP_011509084.1:p.Thr1148Ser
|
|
XM_011510783.1:c.3275C>G
|
XP_011509085.1:p.Thr1092Ser
|
|
XM_011510784.1:c.3272C>G
|
XP_011509086.1:p.Thr1091Ser
|
|
XM_011510785.1:c.3257C>G
|
XP_011509087.1:p.Thr1086Ser
|
|
XM_011510786.1:c.3152C>G
|
XP_011509088.1:p.Thr1051Ser
|
|
XM_011510787.1:c.3149C>G
|
XP_011509089.1:p.Thr1050Ser
|
|
XM_011510788.1:c.3116C>G
|
XP_011509090.1:p.Thr1039Ser
|
|
XM_011510789.1:c.2966C>G
|
XP_011509091.1:p.Thr989Ser
|
|
XM_011510790.1:c.2450C>G
|
XP_011509092.1:p.Thr817Ser
|
|
XM_011510791.1:c.2450C>G
|
XP_011509093.1:p.Thr817Ser
|
|
XM_011510792.1:c.3443C>G
|
XP_011509094.1:p.Thr1148Ser
|
|
XR_922888.1:n.3580C>G
|
|
|
XM_011510778.3:c.3443C>G
|
XP_011509080.1:p.Thr1148Ser
|
|
XM_011510779.2:c.3443C>G
|
XP_011509081.1:p.Thr1148Ser
|
|
XM_011510780.2:c.3440C>G
|
XP_011509082.1:p.Thr1147Ser
|
|
XM_011510781.3:c.3425C>G
|
XP_011509083.1:p.Thr1142Ser
|
|
XM_011510782.3:c.3443C>G
|
XP_011509084.1:p.Thr1148Ser
|
|
XM_011510783.3:c.3275C>G
|
XP_011509085.1:p.Thr1092Ser
|
|
XM_011510784.2:c.3272C>G
|
XP_011509086.1:p.Thr1091Ser
|
|
XM_011510785.3:c.3257C>G
|
XP_011509087.1:p.Thr1086Ser
|
|
XM_011510786.3:c.3152C>G
|
XP_011509088.1:p.Thr1051Ser
|
|
XM_011510789.2:c.2966C>G
|
XP_011509091.1:p.Thr989Ser
|
|
XM_011510792.3:c.3443C>G
|
XP_011509094.1:p.Thr1148Ser
|
|
XM_017003568.1:c.3389C>G
|
XP_016859057.1:p.Thr1130Ser
|
|
XM_017003569.1:c.3221C>G
|
XP_016859058.1:p.Thr1074Ser
|
|
XM_017003570.1:c.2948C>G
|
XP_016859059.1:p.Thr983Ser
|
|
XM_017003571.1:c.2798C>G
|
XP_016859060.1:p.Thr933Ser
|
|
XM_017003572.1:c.2450C>G
|
XP_016859061.1:p.Thr817Ser
|
|
XM_017003573.1:c.2450C>G
|
XP_016859062.1:p.Thr817Ser
|
|
XM_017003574.1:c.2450C>G
|
XP_016859063.1:p.Thr817Ser
|
|
NM_015040.4:c.3407C>G
MANE Select
|
NP_055855.2:p.Thr1136Ser
|
|