ENST00000614565.5:c.576+33561G>T
MANE Select
|
ENSP00000484928.1:n.576+33561G>T
|
|
ENST00000543233.2:c.354+33561G>T
|
ENSP00000443301.1:n.354+33561G>T
|
|
ENST00000611855.4:c.294+33561G>T
|
ENSP00000480844.1:n.294+33561G>T
|
|
ENST00000614565.4:c.576+33561G>T
|
ENSP00000484928.1:n.576+33561G>T
|
|
NM_001252338.2:c.465+33561G>T
|
NP_001239267.1:n.465+33561G>T
|
|
NM_001252339.2:c.354+33561G>T
|
NP_001239268.1:n.354+33561G>T
|
|
NM_001794.4:c.576+33561G>T
|
NP_001785.2:n.576+33561G>T
|
|
NM_001794.5:c.576+33561G>T
MANE Select
|
NP_001785.2:n.576+33561G>T
|
|
NM_001252339.3:c.354+33561G>T
|
NP_001239268.1:n.354+33561G>T
|
|