ENST00000281928.9:c.5107T>C
MANE Select
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ENSP00000281928.3:p.Leu1703=
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ENST00000549786.2:c.4535T>C
|
|
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ENST00000648379.1:n.3475T>C
|
|
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ENST00000648737.1:n.4871T>C
|
|
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ENST00000648825.1:n.1847T>C
|
|
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ENST00000648916.1:n.3118T>C
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|
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ENST00000649146.1:n.2350T>C
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|
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ENST00000649607.1:c.3291T>C
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|
|
ENST00000649775.1:c.1596T>C
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|
|
ENST00000650226.1:c.5107T>C
|
ENSP00000496981.1:p.Leu1703=
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ENST00000281928.7:c.5107T>C
|
ENSP00000281928.3:p.Leu1703=
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|
ENST00000549786.1:c.471T>C
|
|
|
ENST00000552340.1:c.139T>C
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ENSP00000449876.1:p.Leu47=
|
|
NM_015335.4:c.5107T>C
|
NP_056150.1:p.Leu1703=
|
|
XM_011538080.1:c.5107T>C
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XP_011536382.1:p.Leu1703=
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XM_011538081.1:c.5104T>C
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XP_011536383.1:p.Leu1702=
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XM_011538082.1:c.5077T>C
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XP_011536384.1:p.Leu1693=
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|
XM_011538080.2:c.5107T>C
|
XP_011536382.1:p.Leu1703=
|
|
XM_011538081.2:c.5104T>C
|
XP_011536383.1:p.Leu1702=
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|
XM_011538082.2:c.5077T>C
|
XP_011536384.1:p.Leu1693=
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XM_017019090.1:c.5104T>C
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XP_016874579.1:p.Leu1702=
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|
NM_015335.5:c.5107T>C
MANE Select
|
NP_056150.1:p.Leu1703=
|
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