ENST00000682565.1:c.11694C>T
|
ENSP00000507671.1:p.Gly3898=
|
|
ENST00000682801.1:c.11167-788C>T
|
ENSP00000507862.1:n.11167-788C>T
|
|
ENST00000682859.1:c.11694C>T
|
ENSP00000508222.1:p.Gly3898=
|
|
ENST00000683791.1:c.4780C>T
|
|
|
ENST00000684460.1:c.8975C>T
|
|
|
ENST00000684548.1:c.11694C>T
|
ENSP00000507421.1:p.Gly3898=
|
|
ENST00000684590.1:c.6141C>T
|
ENSP00000507376.1:p.Gly2047=
|
|
ENST00000684656.1:c.9159C>T
|
|
|
ENST00000613296.6:c.12075C>T
MANE Select
|
ENSP00000482968.1:p.Gly4025=
|
|
ENST00000651057.1:c.2229C>T
|
ENSP00000498504.1:p.Gly743=
|
|
ENST00000651434.1:c.3431C>T
|
|
|
ENST00000651750.1:c.1260+516C>T
|
|
|
ENST00000652487.1:c.3246C>T
|
|
|
ENST00000464408.3:n.250C>T
|
|
|
ENST00000484298.5:c.11949C>T
|
ENSP00000478155.1:p.Gly3983=
|
|
ENST00000613296.4:c.12075C>T
|
ENSP00000482968.1:p.Gly4025=
|
|
ENST00000620466.4:n.5878C>T
|
|
|
NM_015120.4:c.12078C>T , LRG_741t1:c.12078C>T
|
NP_055935.4:p.Gly4026=
|
|
NM_001378454.1:c.12075C>T
MANE Select
|
NP_001365383.1:p.Gly4025=
|
|