ENST00000704289.1:c.-42G>T
|
ENSP00000515816.1:n.-42G>T
|
|
ENST00000315285.9:c.-42G>T
MANE Select
|
ENSP00000320885.3:n.-42G>T
|
|
ENST00000621856.2:c.-42G>T
|
ENSP00000482496.2:n.-42G>T
|
|
ENST00000646571.1:c.-42G>T
|
ENSP00000495015.1:n.-42G>T
|
|
ENST00000315285.7:c.-42G>T
|
ENSP00000320885.3:n.-42G>T
|
|
ENST00000345662.5:c.-42G>T
|
ENSP00000340817.1:n.-42G>T
|
|
ENST00000615843.4:c.-42G>T
|
ENSP00000480893.1:n.-42G>T
|
|
NM_014946.3:c.-42G>T , LRG_714t1:c.-42G>T
|
NP_055761.2:n.-42G>T
|
|
NM_199436.1:c.-42G>T
|
NP_955468.1:n.-42G>T
|
|
XM_005264516.3:c.-42G>T
|
XP_005264573.1:n.-42G>T
|
|
XM_011533067.1:c.-42G>T
|
XP_011531369.1:n.-42G>T
|
|
NM_001363823.1:c.-42G>T
|
NP_001350752.1:n.-42G>T
|
|
NM_001363875.1:c.-42G>T
|
NP_001350804.1:n.-42G>T
|
|
XM_011533067.2:c.-42G>T
|
XP_011531369.1:n.-42G>T
|
|
XM_017004778.2:c.-42G>T
|
XP_016860267.1:n.-42G>T
|
|
NM_001363823.2:c.-42G>T
|
NP_001350752.1:n.-42G>T
|
|
NM_001363875.2:c.-42G>T
|
NP_001350804.1:n.-42G>T
|
|
NM_001377959.1:c.-42G>T
|
NP_001364888.1:n.-42G>T
|
|
NM_014946.4:c.-42G>T
MANE Select
|
NP_055761.2:n.-42G>T
|
|
NM_199436.2:c.-42G>T
|
NP_955468.1:n.-42G>T
|
|