ENST00000649865.1:c.1345G>T
|
ENSP00000496919.1:p.Ala449Ser
|
|
ENST00000650285.1:c.1345G>T
MANE Select
|
ENSP00000497069.1:p.Ala449Ser
|
|
ENST00000268035.10:c.1345G>T
|
ENSP00000268035.6:p.Ala449Ser
|
|
ENST00000558762.5:c.1345G>T
|
ENSP00000453007.1:p.Ala449Ser
|
|
ENST00000558898.1:c.436G>T
|
ENSP00000454115.1:p.Ala146Ser
|
|
ENST00000559582.1:n.252G>T
|
|
|
ENST00000559925.5:n.1345G>T
|
|
|
NM_000875.4:c.1345G>T
|
NP_000866.1:p.Ala449Ser
|
|
NM_001291858.1:c.1345G>T
|
NP_001278787.1:p.Ala449Ser
|
|
XM_011521513.1:c.1408G>T
|
XP_011519815.1:p.Ala470Ser
|
|
XM_011521514.1:c.1408G>T
|
XP_011519816.1:p.Ala470Ser
|
|
XM_011521515.1:c.1408G>T
|
XP_011519817.1:p.Ala470Ser
|
|
XM_011521516.1:c.436G>T
|
XP_011519818.1:p.Ala146Ser
|
|
XM_011521517.1:c.10G>T
|
XP_011519819.1:p.Ala4Ser
|
|
XM_011521516.2:c.436G>T
|
XP_011519818.1:p.Ala146Ser
|
|
XM_011521517.2:c.10G>T
|
XP_011519819.1:p.Ala4Ser
|
|
XM_017022136.1:c.1420G>T
|
XP_016877625.1:p.Ala474Ser
|
|
XM_017022137.1:c.1420G>T
|
XP_016877626.1:p.Ala474Ser
|
|
XM_017022138.1:c.1420G>T
|
XP_016877627.1:p.Ala474Ser
|
|
XM_017022139.1:c.982G>T
|
XP_016877628.1:p.Ala328Ser
|
|
XM_024449913.1:c.436G>T
|
XP_024305681.1:p.Ala146Ser
|
|
NM_000875.5:c.1345G>T
MANE Select
|
NP_000866.1:p.Ala449Ser
|
|
NM_001291858.2:c.1345G>T
|
NP_001278787.1:p.Ala449Ser
|
|