ENST00000281928.9:c.5944T=
MANE Select
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ENSP00000281928.3:p.Ser1982=
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ENST00000548784.2:n.2158T=
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ENST00000648379.1:n.4312T=
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ENST00000648737.1:n.5708T=
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ENST00000648825.1:n.4129T=
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ENST00000648916.1:n.3955T=
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ENST00000649607.1:c.4128T=
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|
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ENST00000649775.1:c.2433T=
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|
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ENST00000650226.1:c.5980T=
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ENSP00000496981.1:p.Ser1994=
|
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ENST00000281928.7:c.5944T=
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ENSP00000281928.3:p.Ser1982=
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ENST00000548784.1:n.442T=
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|
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ENST00000552447.1:c.557T=
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NM_015335.4:c.5944T=
|
NP_056150.1:p.Ser1982=
|
|
XM_011538080.1:c.5980T=
|
XP_011536382.1:p.Ser1994=
|
|
XM_011538081.1:c.5977T=
|
XP_011536383.1:p.Ser1993=
|
|
XM_011538082.1:c.5950T=
|
XP_011536384.1:p.Ser1984=
|
|
XM_011538080.2:c.5980T=
|
XP_011536382.1:p.Ser1994=
|
|
XM_011538081.2:c.5977T=
|
XP_011536383.1:p.Ser1993=
|
|
XM_011538082.2:c.5950T=
|
XP_011536384.1:p.Ser1984=
|
|
XM_017019090.1:c.5941T=
|
XP_016874579.1:p.Ser1981=
|
|
NM_015335.5:c.5944T=
MANE Select
|
NP_056150.1:p.Ser1982=
|
|