ENST00000281928.9:c.5015C>A
MANE Select
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ENSP00000281928.3:p.Ala1672Asp
|
|
ENST00000549786.2:c.4443C>A
|
|
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ENST00000648379.1:n.3383C>A
|
|
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ENST00000648737.1:n.4779C>A
|
|
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ENST00000648825.1:n.1755C>A
|
|
|
ENST00000648916.1:n.3026C>A
|
|
|
ENST00000649146.1:n.2258C>A
|
|
|
ENST00000649607.1:c.3199C>A
|
|
|
ENST00000649775.1:c.1504C>A
|
|
|
ENST00000650226.1:c.5015C>A
|
ENSP00000496981.1:p.Ala1672Asp
|
|
ENST00000281928.7:c.5015C>A
|
ENSP00000281928.3:p.Ala1672Asp
|
|
ENST00000549786.1:c.379C>A
|
|
|
ENST00000552340.1:c.47C>A
|
ENSP00000449876.1:p.Ala16Asp
|
|
NM_015335.4:c.5015C>A
|
NP_056150.1:p.Ala1672Asp
|
|
XM_011538080.1:c.5015C>A
|
XP_011536382.1:p.Ala1672Asp
|
|
XM_011538081.1:c.5012C>A
|
XP_011536383.1:p.Ala1671Asp
|
|
XM_011538082.1:c.4985C>A
|
XP_011536384.1:p.Ala1662Asp
|
|
XM_011538080.2:c.5015C>A
|
XP_011536382.1:p.Ala1672Asp
|
|
XM_011538081.2:c.5012C>A
|
XP_011536383.1:p.Ala1671Asp
|
|
XM_011538082.2:c.4985C>A
|
XP_011536384.1:p.Ala1662Asp
|
|
XM_017019090.1:c.5012C>A
|
XP_016874579.1:p.Ala1671Asp
|
|
NM_015335.5:c.5015C>A
MANE Select
|
NP_056150.1:p.Ala1672Asp
|
|