ENST00000264380.9:c.3443T>C
MANE Select
|
ENSP00000264380.4:p.Leu1148Ser
|
|
ENST00000264380.8:c.3443T>C
|
ENSP00000264380.4:p.Leu1148Ser
|
|
ENST00000452564.1:c.3275T>C
|
ENSP00000405736.1:p.Leu1092Ser
|
|
NM_015040.3:c.3443T>C
|
NP_055855.2:p.Leu1148Ser
|
|
XM_011510778.1:c.3479T>C
|
XP_011509080.1:p.Leu1160Ser
|
|
XM_011510779.1:c.3479T>C
|
XP_011509081.1:p.Leu1160Ser
|
|
XM_011510780.1:c.3476T>C
|
XP_011509082.1:p.Leu1159Ser
|
|
XM_011510781.1:c.3461T>C
|
XP_011509083.1:p.Leu1154Ser
|
|
XM_011510782.1:c.3479T>C
|
XP_011509084.1:p.Leu1160Ser
|
|
XM_011510783.1:c.3311T>C
|
XP_011509085.1:p.Leu1104Ser
|
|
XM_011510784.1:c.3308T>C
|
XP_011509086.1:p.Leu1103Ser
|
|
XM_011510785.1:c.3293T>C
|
XP_011509087.1:p.Leu1098Ser
|
|
XM_011510786.1:c.3188T>C
|
XP_011509088.1:p.Leu1063Ser
|
|
XM_011510787.1:c.3185T>C
|
XP_011509089.1:p.Leu1062Ser
|
|
XM_011510788.1:c.3152T>C
|
XP_011509090.1:p.Leu1051Ser
|
|
XM_011510789.1:c.3002T>C
|
XP_011509091.1:p.Leu1001Ser
|
|
XM_011510790.1:c.2486T>C
|
XP_011509092.1:p.Leu829Ser
|
|
XM_011510791.1:c.2486T>C
|
XP_011509093.1:p.Leu829Ser
|
|
XM_011510792.1:c.3479T>C
|
XP_011509094.1:p.Leu1160Ser
|
|
XR_922888.1:n.3616T>C
|
|
|
XM_011510778.3:c.3479T>C
|
XP_011509080.1:p.Leu1160Ser
|
|
XM_011510779.2:c.3479T>C
|
XP_011509081.1:p.Leu1160Ser
|
|
XM_011510780.2:c.3476T>C
|
XP_011509082.1:p.Leu1159Ser
|
|
XM_011510781.3:c.3461T>C
|
XP_011509083.1:p.Leu1154Ser
|
|
XM_011510782.3:c.3479T>C
|
XP_011509084.1:p.Leu1160Ser
|
|
XM_011510783.3:c.3311T>C
|
XP_011509085.1:p.Leu1104Ser
|
|
XM_011510784.2:c.3308T>C
|
XP_011509086.1:p.Leu1103Ser
|
|
XM_011510785.3:c.3293T>C
|
XP_011509087.1:p.Leu1098Ser
|
|
XM_011510786.3:c.3188T>C
|
XP_011509088.1:p.Leu1063Ser
|
|
XM_011510789.2:c.3002T>C
|
XP_011509091.1:p.Leu1001Ser
|
|
XM_011510792.3:c.3479T>C
|
XP_011509094.1:p.Leu1160Ser
|
|
XM_017003568.1:c.3425T>C
|
XP_016859057.1:p.Leu1142Ser
|
|
XM_017003569.1:c.3257T>C
|
XP_016859058.1:p.Leu1086Ser
|
|
XM_017003570.1:c.2984T>C
|
XP_016859059.1:p.Leu995Ser
|
|
XM_017003571.1:c.2834T>C
|
XP_016859060.1:p.Leu945Ser
|
|
XM_017003572.1:c.2486T>C
|
XP_016859061.1:p.Leu829Ser
|
|
XM_017003573.1:c.2486T>C
|
XP_016859062.1:p.Leu829Ser
|
|
XM_017003574.1:c.2486T>C
|
XP_016859063.1:p.Leu829Ser
|
|
NM_015040.4:c.3443T>C
MANE Select
|
NP_055855.2:p.Leu1148Ser
|
|