ENST00000302746.11:c.572T>G
MANE Select
|
ENSP00000307241.6:p.Ile191Ser
|
|
ENST00000302746.10:c.572T>G
|
ENSP00000307241.6:p.Ile191Ser
|
|
ENST00000383714.8:c.518T>G
|
ENSP00000373220.4:p.Ile173Ser
|
|
ENST00000461692.5:n.685T>G
|
|
|
ENST00000469364.5:c.572T>G
|
ENSP00000419580.1:p.Ile191Ser
|
|
ENST00000474765.1:c.518T>G
|
ENSP00000418448.1:p.Ile173Ser
|
|
ENST00000479945.1:n.2977T>G
|
|
|
ENST00000480626.5:n.664T>G
|
|
|
ENST00000485460.5:c.518T>G
|
ENSP00000417267.1:p.Ile173Ser
|
|
NM_000925.3:c.572T>G
|
NP_000916.2:p.Ile191Ser
|
|
NM_001173468.1:c.518T>G
|
NP_001166939.1:p.Ile173Ser
|
|
NM_001315536.1:c.518T>G
|
NP_001302465.1:p.Ile173Ser
|
|
NR_033384.1:n.685T>G
|
|
|
NM_000925.4:c.572T>G
MANE Select
|
NP_000916.2:p.Ile191Ser
|
|
NM_001173468.2:c.518T>G
|
NP_001166939.1:p.Ile173Ser
|
|
NM_001315536.2:c.518T>G
|
NP_001302465.1:p.Ile173Ser
|
|
NR_033384.2:n.678T>G
|
|
|