ENST00000636937.2:c.1855G>T
|
ENSP00000516154.1:p.Gly619Cys
|
|
ENST00000268124.11:c.1855G>T
MANE Select
|
ENSP00000268124.5:p.Gly619Cys
|
|
ENST00000530292.3:c.1456G>T
|
ENSP00000432885.2:p.Gly486Cys
|
|
ENST00000635986.2:c.1855G>T
|
ENSP00000490653.2:p.Gly619Cys
|
|
ENST00000636774.1:c.*422G>T
|
ENSP00000489799.1:n.*422G>T
|
|
ENST00000637238.1:c.592G>T
|
ENSP00000490756.1:p.Gly198Cys
|
|
ENST00000637264.1:c.927G>T
|
|
|
ENST00000666746.1:c.1432G>T
|
|
|
ENST00000670281.1:c.175G>T
|
ENSP00000499709.1:p.Gly59Cys
|
|
ENST00000672071.1:n.2053G>T
|
|
|
ENST00000672923.2:n.1958G>T
|
|
|
ENST00000268124.9:c.1855G>T
|
ENSP00000268124.5:p.Gly619Cys
|
|
ENST00000442287.6:c.1855G>T
|
ENSP00000399851.2:p.Gly619Cys
|
|
ENST00000526314.2:c.237G>T
|
|
|
ENST00000526398.1:c.44G>T
|
|
|
ENST00000532584.5:n.57G>T
|
|
|
ENST00000631044.2:c.*1238G>T
|
ENSP00000486730.1:n.*1238G>T
|
|
NM_001126131.1:c.1855G>T
|
NP_001119603.1:p.Gly619Cys
|
|
NM_002693.2:c.1855G>T
|
NP_002684.1:p.Gly619Cys
|
|
NM_001126131.2:c.1855G>T
|
NP_001119603.1:p.Gly619Cys
|
|
NM_002693.3:c.1855G>T
MANE Select
|
NP_002684.1:p.Gly619Cys
|
|