ENST00000281928.9:c.4983T>C
MANE Select
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ENSP00000281928.3:p.Ile1661=
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ENST00000549786.2:c.4411T>C
|
|
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ENST00000648379.1:n.3351T>C
|
|
|
ENST00000648737.1:n.4747T>C
|
|
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ENST00000648825.1:n.1723T>C
|
|
|
ENST00000648916.1:n.2994T>C
|
|
|
ENST00000649146.1:n.2226T>C
|
|
|
ENST00000649607.1:c.3167T>C
|
|
|
ENST00000649775.1:c.1472T>C
|
|
|
ENST00000650226.1:c.4983T>C
|
ENSP00000496981.1:p.Ile1661=
|
|
ENST00000281928.7:c.4983T>C
|
ENSP00000281928.3:p.Ile1661=
|
|
ENST00000549786.1:c.347T>C
|
|
|
ENST00000552340.1:c.15T>C
|
ENSP00000449876.1:p.Ile5=
|
|
NM_015335.4:c.4983T>C
|
NP_056150.1:p.Ile1661=
|
|
XM_011538080.1:c.4983T>C
|
XP_011536382.1:p.Ile1661=
|
|
XM_011538081.1:c.4980T>C
|
XP_011536383.1:p.Ile1660=
|
|
XM_011538082.1:c.4953T>C
|
XP_011536384.1:p.Ile1651=
|
|
XM_011538080.2:c.4983T>C
|
XP_011536382.1:p.Ile1661=
|
|
XM_011538081.2:c.4980T>C
|
XP_011536383.1:p.Ile1660=
|
|
XM_011538082.2:c.4953T>C
|
XP_011536384.1:p.Ile1651=
|
|
XM_017019090.1:c.4980T>C
|
XP_016874579.1:p.Ile1660=
|
|
NM_015335.5:c.4983T>C
MANE Select
|
NP_056150.1:p.Ile1661=
|
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