ENST00000281928.9:c.5929G=
MANE Select
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ENSP00000281928.3:p.Ala1977=
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ENST00000548784.2:n.2143G=
|
|
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ENST00000648379.1:n.4297G=
|
|
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ENST00000648737.1:n.5693G=
|
|
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ENST00000648825.1:n.4114G=
|
|
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ENST00000648916.1:n.3940G=
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|
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ENST00000649607.1:c.4113G=
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|
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ENST00000649775.1:c.2418G=
|
|
|
ENST00000650226.1:c.5965G=
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ENSP00000496981.1:p.Ala1989=
|
|
ENST00000281928.7:c.5929G=
|
ENSP00000281928.3:p.Ala1977=
|
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ENST00000548784.1:n.427G=
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|
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ENST00000552447.1:c.542G=
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|
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NM_015335.4:c.5929G=
|
NP_056150.1:p.Ala1977=
|
|
XM_011538080.1:c.5965G=
|
XP_011536382.1:p.Ala1989=
|
|
XM_011538081.1:c.5962G=
|
XP_011536383.1:p.Ala1988=
|
|
XM_011538082.1:c.5935G=
|
XP_011536384.1:p.Ala1979=
|
|
XM_011538080.2:c.5965G=
|
XP_011536382.1:p.Ala1989=
|
|
XM_011538081.2:c.5962G=
|
XP_011536383.1:p.Ala1988=
|
|
XM_011538082.2:c.5935G=
|
XP_011536384.1:p.Ala1979=
|
|
XM_017019090.1:c.5926G=
|
XP_016874579.1:p.Ala1976=
|
|
NM_015335.5:c.5929G=
MANE Select
|
NP_056150.1:p.Ala1977=
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