ENST00000475778.2:n.688T>G
|
|
|
ENST00000683214.1:n.544+14001T>G
|
|
|
ENST00000684143.1:c.262T>G
|
ENSP00000508264.1:p.Trp88Gly
|
|
ENST00000379374.5:c.262T>G
MANE Select
|
ENSP00000368682.4:p.Trp88Gly
|
|
ENST00000379374.4:c.262T>G
|
ENSP00000368682.4:p.Trp88Gly
|
|
NM_000444.5:c.262T>G
|
NP_000435.3:p.Trp88Gly
|
|
NM_001282754.1:c.262T>G
|
NP_001269683.1:p.Trp88Gly
|
|
XM_011545535.1:c.262T>G
|
XP_011543837.1:p.Trp88Gly
|
|
XM_024452390.1:c.-30T>G
|
XP_024308158.1:n.-30T>G
|
|
XR_001755695.1:n.941T>G
|
|
|
NM_000444.6:c.262T>G
MANE Select
|
NP_000435.3:p.Trp88Gly
|
|
NM_001282754.2:c.262T>G
|
NP_001269683.1:p.Trp88Gly
|
|