ENST00000682565.1:c.11672C>G
|
ENSP00000507671.1:p.Ala3891Gly
|
|
ENST00000682801.1:c.11167-810C>G
|
ENSP00000507862.1:n.11167-810C>G
|
|
ENST00000682859.1:c.11672C>G
|
ENSP00000508222.1:p.Ala3891Gly
|
|
ENST00000683791.1:c.4758C>G
|
|
|
ENST00000684460.1:c.8953C>G
|
|
|
ENST00000684548.1:c.11672C>G
|
ENSP00000507421.1:p.Ala3891Gly
|
|
ENST00000684590.1:c.6119C>G
|
ENSP00000507376.1:p.Ala2040Gly
|
|
ENST00000684656.1:c.9137C>G
|
|
|
ENST00000613296.6:c.12053C>G
MANE Select
|
ENSP00000482968.1:p.Ala4018Gly
|
|
ENST00000651057.1:c.2207C>G
|
ENSP00000498504.1:p.Ala736Gly
|
|
ENST00000651434.1:c.3409C>G
|
|
|
ENST00000651750.1:c.1260+494C>G
|
|
|
ENST00000652487.1:c.3224C>G
|
|
|
ENST00000464408.3:n.228C>G
|
|
|
ENST00000484298.5:c.11927C>G
|
ENSP00000478155.1:p.Ala3976Gly
|
|
ENST00000613296.4:c.12053C>G
|
ENSP00000482968.1:p.Ala4018Gly
|
|
ENST00000620466.4:n.5856C>G
|
|
|
NM_015120.4:c.12056C>G , LRG_741t1:c.12056C>G
|
NP_055935.4:p.Ala4019Gly
|
|
NM_001378454.1:c.12053C>G
MANE Select
|
NP_001365383.1:p.Ala4018Gly
|
|