ENST00000264380.9:c.3444G>C
MANE Select
|
ENSP00000264380.4:p.Leu1148Phe
|
|
ENST00000264380.8:c.3444G>C
|
ENSP00000264380.4:p.Leu1148Phe
|
|
ENST00000452564.1:c.3276G>C
|
ENSP00000405736.1:p.Leu1092Phe
|
|
NM_015040.3:c.3444G>C
|
NP_055855.2:p.Leu1148Phe
|
|
XM_011510778.1:c.3480G>C
|
XP_011509080.1:p.Leu1160Phe
|
|
XM_011510779.1:c.3480G>C
|
XP_011509081.1:p.Leu1160Phe
|
|
XM_011510780.1:c.3477G>C
|
XP_011509082.1:p.Leu1159Phe
|
|
XM_011510781.1:c.3462G>C
|
XP_011509083.1:p.Leu1154Phe
|
|
XM_011510782.1:c.3480G>C
|
XP_011509084.1:p.Leu1160Phe
|
|
XM_011510783.1:c.3312G>C
|
XP_011509085.1:p.Leu1104Phe
|
|
XM_011510784.1:c.3309G>C
|
XP_011509086.1:p.Leu1103Phe
|
|
XM_011510785.1:c.3294G>C
|
XP_011509087.1:p.Leu1098Phe
|
|
XM_011510786.1:c.3189G>C
|
XP_011509088.1:p.Leu1063Phe
|
|
XM_011510787.1:c.3186G>C
|
XP_011509089.1:p.Leu1062Phe
|
|
XM_011510788.1:c.3153G>C
|
XP_011509090.1:p.Leu1051Phe
|
|
XM_011510789.1:c.3003G>C
|
XP_011509091.1:p.Leu1001Phe
|
|
XM_011510790.1:c.2487G>C
|
XP_011509092.1:p.Leu829Phe
|
|
XM_011510791.1:c.2487G>C
|
XP_011509093.1:p.Leu829Phe
|
|
XM_011510792.1:c.3480G>C
|
XP_011509094.1:p.Leu1160Phe
|
|
XR_922888.1:n.3617G>C
|
|
|
XM_011510778.3:c.3480G>C
|
XP_011509080.1:p.Leu1160Phe
|
|
XM_011510779.2:c.3480G>C
|
XP_011509081.1:p.Leu1160Phe
|
|
XM_011510780.2:c.3477G>C
|
XP_011509082.1:p.Leu1159Phe
|
|
XM_011510781.3:c.3462G>C
|
XP_011509083.1:p.Leu1154Phe
|
|
XM_011510782.3:c.3480G>C
|
XP_011509084.1:p.Leu1160Phe
|
|
XM_011510783.3:c.3312G>C
|
XP_011509085.1:p.Leu1104Phe
|
|
XM_011510784.2:c.3309G>C
|
XP_011509086.1:p.Leu1103Phe
|
|
XM_011510785.3:c.3294G>C
|
XP_011509087.1:p.Leu1098Phe
|
|
XM_011510786.3:c.3189G>C
|
XP_011509088.1:p.Leu1063Phe
|
|
XM_011510789.2:c.3003G>C
|
XP_011509091.1:p.Leu1001Phe
|
|
XM_011510792.3:c.3480G>C
|
XP_011509094.1:p.Leu1160Phe
|
|
XM_017003568.1:c.3426G>C
|
XP_016859057.1:p.Leu1142Phe
|
|
XM_017003569.1:c.3258G>C
|
XP_016859058.1:p.Leu1086Phe
|
|
XM_017003570.1:c.2985G>C
|
XP_016859059.1:p.Leu995Phe
|
|
XM_017003571.1:c.2835G>C
|
XP_016859060.1:p.Leu945Phe
|
|
XM_017003572.1:c.2487G>C
|
XP_016859061.1:p.Leu829Phe
|
|
XM_017003573.1:c.2487G>C
|
XP_016859062.1:p.Leu829Phe
|
|
XM_017003574.1:c.2487G>C
|
XP_016859063.1:p.Leu829Phe
|
|
NM_015040.4:c.3444G>C
MANE Select
|
NP_055855.2:p.Leu1148Phe
|
|