ENST00000682565.1:c.11554A>C
|
ENSP00000507671.1:p.Asn3852His
|
|
ENST00000682801.1:c.11167-928A>C
|
ENSP00000507862.1:n.11167-928A>C
|
|
ENST00000682859.1:c.11554A>C
|
ENSP00000508222.1:p.Asn3852His
|
|
ENST00000683791.1:c.4640A>C
|
|
|
ENST00000684460.1:c.8835A>C
|
|
|
ENST00000684548.1:c.11554A>C
|
ENSP00000507421.1:p.Asn3852His
|
|
ENST00000684590.1:c.6001A>C
|
ENSP00000507376.1:p.Asn2001His
|
|
ENST00000684656.1:c.9019A>C
|
|
|
ENST00000613296.6:c.11935A>C
MANE Select
|
ENSP00000482968.1:p.Asn3979His
|
|
ENST00000651057.1:c.2089A>C
|
ENSP00000498504.1:p.Asn697His
|
|
ENST00000651434.1:c.3291A>C
|
|
|
ENST00000651750.1:c.1260+376A>C
|
|
|
ENST00000652487.1:c.3106A>C
|
|
|
ENST00000464408.3:n.110A>C
|
|
|
ENST00000484298.5:c.11809A>C
|
ENSP00000478155.1:p.Asn3937His
|
|
ENST00000613296.4:c.11935A>C
|
ENSP00000482968.1:p.Asn3979His
|
|
ENST00000620466.4:n.5738A>C
|
|
|
NM_015120.4:c.11938A>C , LRG_741t1:c.11938A>C
|
NP_055935.4:p.Asn3980His
|
|
NM_001378454.1:c.11935A>C
MANE Select
|
NP_001365383.1:p.Asn3979His
|
|