ENST00000281928.9:c.2682A=
MANE Select
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ENSP00000281928.3:p.Ala894=
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ENST00000548743.2:c.2652A=
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ENSP00000448553.2:p.Ala884=
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|
ENST00000549786.2:c.2110A=
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|
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ENST00000647927.1:n.3055A=
|
|
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ENST00000648173.1:n.1477A=
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|
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ENST00000648379.1:n.1050A=
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|
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ENST00000648737.1:n.2446A=
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|
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ENST00000648916.1:n.693A=
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|
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ENST00000649607.1:c.866A=
|
|
|
ENST00000650226.1:c.2682A=
|
ENSP00000496981.1:p.Ala894=
|
|
ENST00000281928.7:c.2682A=
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ENSP00000281928.3:p.Ala894=
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|
NM_015335.4:c.2682A=
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NP_056150.1:p.Ala894=
|
|
XM_011538080.1:c.2682A=
|
XP_011536382.1:p.Ala894=
|
|
XM_011538081.1:c.2679A=
|
XP_011536383.1:p.Ala893=
|
|
XM_011538082.1:c.2652A=
|
XP_011536384.1:p.Ala884=
|
|
XM_011538080.2:c.2682A=
|
XP_011536382.1:p.Ala894=
|
|
XM_011538081.2:c.2679A=
|
XP_011536383.1:p.Ala893=
|
|
XM_011538082.2:c.2652A=
|
XP_011536384.1:p.Ala884=
|
|
XM_017019090.1:c.2679A=
|
XP_016874579.1:p.Ala893=
|
|
NM_015335.5:c.2682A=
MANE Select
|
NP_056150.1:p.Ala894=
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