ENST00000682565.1:c.11680G>T
|
ENSP00000507671.1:p.Gly3894Cys
|
|
ENST00000682801.1:c.11167-802G>T
|
ENSP00000507862.1:n.11167-802G>T
|
|
ENST00000682859.1:c.11680G>T
|
ENSP00000508222.1:p.Gly3894Cys
|
|
ENST00000683791.1:c.4766G>T
|
|
|
ENST00000684460.1:c.8961G>T
|
|
|
ENST00000684548.1:c.11680G>T
|
ENSP00000507421.1:p.Gly3894Cys
|
|
ENST00000684590.1:c.6127G>T
|
ENSP00000507376.1:p.Gly2043Cys
|
|
ENST00000684656.1:c.9145G>T
|
|
|
ENST00000613296.6:c.12061G>T
MANE Select
|
ENSP00000482968.1:p.Gly4021Cys
|
|
ENST00000651057.1:c.2215G>T
|
ENSP00000498504.1:p.Gly739Cys
|
|
ENST00000651434.1:c.3417G>T
|
|
|
ENST00000651750.1:c.1260+502G>T
|
|
|
ENST00000652487.1:c.3232G>T
|
|
|
ENST00000464408.3:n.236G>T
|
|
|
ENST00000484298.5:c.11935G>T
|
ENSP00000478155.1:p.Gly3979Cys
|
|
ENST00000613296.4:c.12061G>T
|
ENSP00000482968.1:p.Gly4021Cys
|
|
ENST00000620466.4:n.5864G>T
|
|
|
NM_015120.4:c.12064G>T , LRG_741t1:c.12064G>T
|
NP_055935.4:p.Gly4022Cys
|
|
NM_001378454.1:c.12061G>T
MANE Select
|
NP_001365383.1:p.Gly4021Cys
|
|