ENST00000682565.1:c.11666A>T
|
ENSP00000507671.1:p.Tyr3889Phe
|
|
ENST00000682801.1:c.11167-816A>T
|
ENSP00000507862.1:n.11167-816A>T
|
|
ENST00000682859.1:c.11666A>T
|
ENSP00000508222.1:p.Tyr3889Phe
|
|
ENST00000683791.1:c.4752A>T
|
|
|
ENST00000684460.1:c.8947A>T
|
|
|
ENST00000684548.1:c.11666A>T
|
ENSP00000507421.1:p.Tyr3889Phe
|
|
ENST00000684590.1:c.6113A>T
|
ENSP00000507376.1:p.Tyr2038Phe
|
|
ENST00000684656.1:c.9131A>T
|
|
|
ENST00000613296.6:c.12047A>T
MANE Select
|
ENSP00000482968.1:p.Tyr4016Phe
|
|
ENST00000651057.1:c.2201A>T
|
ENSP00000498504.1:p.Tyr734Phe
|
|
ENST00000651434.1:c.3403A>T
|
|
|
ENST00000651750.1:c.1260+488A>T
|
|
|
ENST00000652487.1:c.3218A>T
|
|
|
ENST00000464408.3:n.222A>T
|
|
|
ENST00000484298.5:c.11921A>T
|
ENSP00000478155.1:p.Tyr3974Phe
|
|
ENST00000613296.4:c.12047A>T
|
ENSP00000482968.1:p.Tyr4016Phe
|
|
ENST00000620466.4:n.5850A>T
|
|
|
NM_015120.4:c.12050A>T , LRG_741t1:c.12050A>T
|
NP_055935.4:p.Tyr4017Phe
|
|
NM_001378454.1:c.12047A>T
MANE Select
|
NP_001365383.1:p.Tyr4016Phe
|
|