NM_005504.7:c.1066G>A
MANE Select
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NP_005495.2:p.Glu356Lys
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ENST00000261192.12:c.1066G>A
MANE Select
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ENSP00000261192.7:p.Glu356Lys
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NM_001178091.1:c.955G>A
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NP_001171562.1:p.Glu319Lys
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NM_001178091.2:c.955G>A
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NP_001171562.1:p.Glu319Lys
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NM_001178092.1:c.883G>A
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NP_001171563.1:p.Glu295Lys
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NM_001178092.2:c.883G>A
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NP_001171563.1:p.Glu295Lys
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NM_001178093.1:c.1102G>A
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NP_001171564.1:p.Glu368Lys
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NM_001178093.2:c.1102G>A
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NP_001171564.1:p.Glu368Lys
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NM_001178094.1:c.1063G>A
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NP_001171565.1:p.Glu355Lys
|
NM_001178094.2:c.1063G>A
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NP_001171565.1:p.Glu355Lys
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NM_005504.6:c.1066G>A
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NP_005495.2:p.Glu356Lys
|
ENST00000261192.11:c.1066G>A
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ENSP00000261192.7:p.Glu356Lys
|
ENST00000342945.9:c.883G>A
|
ENSP00000339805.5:p.Glu295Lys
|
ENST00000538118.5:c.1063G>A
|
ENSP00000440817.1:p.Glu355Lys
|
ENST00000539282.5:c.1102G>A
|
ENSP00000443459.1:p.Glu368Lys
|
ENST00000539780.5:c.955G>A
|
ENSP00000440827.1:p.Glu319Lys
|
ENST00000543099.1:n.121G>A
|
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XM_011520810.1:c.1102G>A
|
XP_011519112.1:p.Glu368Lys
|
XM_017019768.2:c.1168G>A
|
XP_016875257.1:p.Glu390Lys
|
XR_001748835.2:n.4118G>A
|
|
XR_001749047.1:n.3978-825C>T
|
|
XR_001749048.2:n.3978-825C>T
|
|
XR_001749049.1:n.3885-825C>T
|
|
XR_931441.1:n.1532-825C>T
|
|
XR_931442.1:n.1532-825C>T
|
|
XR_931443.1:n.1439-825C>T
|
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