ENST00000374737.9:c.*402G>T
MANE Select
|
ENSP00000363869.4:n.*402G>T
|
|
ENST00000651578.1:c.*852G>T
|
ENSP00000498502.1:n.*852G>T
|
|
ENST00000374737.8:c.*402G>T
|
ENSP00000363869.4:n.*402G>T
|
|
ENST00000412866.2:c.*402G>T
|
ENSP00000394143.2:n.*402G>T
|
|
ENST00000427538.5:c.1047G>T
|
|
|
ENST00000455586.6:c.*976G>T
|
ENSP00000411581.2:n.*976G>T
|
|
NM_001100431.1:c.*402G>T
|
NP_001093901.1:n.*402G>T
|
|
NM_001184830.1:c.*976G>T
|
NP_001171759.1:n.*976G>T
|
|
NM_001184831.1:c.*976G>T
|
NP_001171760.1:n.*976G>T
|
|
NM_001257403.1:c.*224G>T
|
NP_001244332.1:n.*224G>T
|
|
NM_007268.2:c.*402G>T
|
NP_009199.1:n.*402G>T
|
|
XM_017029251.2:c.*224G>T
|
XP_016884740.1:n.*224G>T
|
|
NM_007268.3:c.*402G>T
MANE Select
|
NP_009199.1:n.*402G>T
|
|
NM_001100431.2:c.*402G>T
|
NP_001093901.1:n.*402G>T
|
|
NM_001184831.2:c.*976G>T
|
NP_001171760.1:n.*976G>T
|
|
NM_001257403.2:c.*224G>T
|
NP_001244332.1:n.*224G>T
|
|
NM_001184830.2:c.*976G>T
|
NP_001171759.1:n.*976G>T
|
|