ENST00000682565.1:c.10343G>T
|
ENSP00000507671.1:p.Gly3448Val
|
|
ENST00000682801.1:c.10343G>T
|
ENSP00000507862.1:p.Gly3448Val
|
|
ENST00000682859.1:c.10343G>T
|
ENSP00000508222.1:p.Gly3448Val
|
|
ENST00000683791.1:c.3429G>T
|
|
|
ENST00000684460.1:c.7624G>T
|
|
|
ENST00000684548.1:c.10343G>T
|
ENSP00000507421.1:p.Gly3448Val
|
|
ENST00000684590.1:c.4790G>T
|
ENSP00000507376.1:p.Gly1597Val
|
|
ENST00000684656.1:c.7669G>T
|
|
|
ENST00000613296.6:c.10724G>T
MANE Select
|
ENSP00000482968.1:p.Gly3575Val
|
|
ENST00000651057.1:c.878G>T
|
ENSP00000498504.1:p.Gly293Val
|
|
ENST00000651434.1:c.2080G>T
|
|
|
ENST00000651750.1:c.112G>T
|
|
|
ENST00000652487.1:c.1821G>T
|
|
|
ENST00000423048.5:c.4215G>T
|
ENSP00000399833.1:n.4215G>T
|
|
ENST00000484298.5:c.10598G>T
|
ENSP00000478155.1:p.Gly3533Val
|
|
ENST00000613296.4:c.10724G>T
|
ENSP00000482968.1:p.Gly3575Val
|
|
ENST00000614410.4:c.10724G>T
|
ENSP00000479094.1:p.Gly3575Val
|
|
ENST00000620466.4:n.4527G>T
|
|
|
NM_015120.4:c.10727G>T , LRG_741t1:c.10727G>T
|
NP_055935.4:p.Gly3576Val
|
|
NM_001378454.1:c.10724G>T
MANE Select
|
NP_001365383.1:p.Gly3575Val
|
|