ENST00000682565.1:c.7843T>G
|
ENSP00000507671.1:p.Cys2615Gly
|
|
ENST00000682801.1:c.7843T>G
|
ENSP00000507862.1:p.Cys2615Gly
|
|
ENST00000682859.1:c.7843T>G
|
ENSP00000508222.1:p.Cys2615Gly
|
|
ENST00000683791.1:c.1235T>G
|
|
|
ENST00000684460.1:c.5295T>G
|
|
|
ENST00000684548.1:c.7843T>G
|
ENSP00000507421.1:p.Cys2615Gly
|
|
ENST00000684590.1:c.2290T>G
|
ENSP00000507376.1:p.Cys764Gly
|
|
ENST00000684656.1:c.5295T>G
|
|
|
ENST00000613296.6:c.8224T>G
MANE Select
|
ENSP00000482968.1:p.Cys2742Gly
|
|
ENST00000651434.1:c.896-29592T>G
|
|
|
ENST00000423048.5:c.3030+25T>G
|
ENSP00000399833.1:n.3030+25T>G
|
|
ENST00000484298.5:c.8098T>G
|
ENSP00000478155.1:p.Cys2700Gly
|
|
ENST00000613296.4:c.8224T>G
|
ENSP00000482968.1:p.Cys2742Gly
|
|
ENST00000614410.4:c.8224T>G
|
ENSP00000479094.1:p.Cys2742Gly
|
|
ENST00000620466.4:n.2027T>G
|
|
|
NM_015120.4:c.8227T>G , LRG_741t1:c.8227T>G
|
NP_055935.4:p.Cys2743Gly
|
|
NM_001378454.1:c.8224T>G
MANE Select
|
NP_001365383.1:p.Cys2742Gly
|
|