ENST00000281928.9:c.2662A=
MANE Select
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ENSP00000281928.3:p.Ser888=
|
|
ENST00000548743.2:c.2632A=
|
ENSP00000448553.2:p.Ser878=
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|
ENST00000549786.2:c.2090A=
|
|
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ENST00000647927.1:n.3035A=
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ENST00000648173.1:n.1457A=
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ENST00000648379.1:n.1030A=
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ENST00000648737.1:n.2426A=
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ENST00000648916.1:n.673A=
|
|
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ENST00000649607.1:c.846A=
|
|
|
ENST00000650226.1:c.2662A=
|
ENSP00000496981.1:p.Ser888=
|
|
ENST00000281928.7:c.2662A=
|
ENSP00000281928.3:p.Ser888=
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|
NM_015335.4:c.2662A=
|
NP_056150.1:p.Ser888=
|
|
XM_011538080.1:c.2662A=
|
XP_011536382.1:p.Ser888=
|
|
XM_011538081.1:c.2659A=
|
XP_011536383.1:p.Ser887=
|
|
XM_011538082.1:c.2632A=
|
XP_011536384.1:p.Ser878=
|
|
XM_011538080.2:c.2662A=
|
XP_011536382.1:p.Ser888=
|
|
XM_011538081.2:c.2659A=
|
XP_011536383.1:p.Ser887=
|
|
XM_011538082.2:c.2632A=
|
XP_011536384.1:p.Ser878=
|
|
XM_017019090.1:c.2659A=
|
XP_016874579.1:p.Ser887=
|
|
NM_015335.5:c.2662A=
MANE Select
|
NP_056150.1:p.Ser888=
|
|