ENST00000317799.10:c.1284C>A
MANE Select
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ENSP00000325136.5:p.His428Gln
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ENST00000317799.9:c.1284C>A
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ENSP00000325136.5:p.His428Gln
|
|
ENST00000405867.7:c.915C>A
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ENSP00000385411.3:p.His305Gln
|
|
ENST00000494615.1:n.2231C>A
|
|
|
ENST00000537713.5:c.1239C>A
|
ENSP00000444295.1:p.His413Gln
|
|
ENST00000545822.2:c.1218C>A
|
ENSP00000442665.1:p.His406Gln
|
|
NM_000183.2:c.1284C>A
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NP_000174.1:p.His428Gln
|
|
NM_001281512.1:c.1239C>A
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NP_001268441.1:p.His413Gln
|
|
NM_001281513.1:c.1218C>A
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NP_001268442.1:p.His406Gln
|
|
XM_011532803.1:c.1284C>A
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XP_011531105.1:p.His428Gln
|
|
XM_011532804.1:c.1218C>A
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XP_011531106.1:p.His406Gln
|
|
XM_024452830.1:c.1254C>A
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XP_024308598.1:p.His418Gln
|
|
XM_024452831.1:c.1218C>A
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XP_024308599.1:p.His406Gln
|
|
NM_000183.3:c.1284C>A
MANE Select
|
NP_000174.1:p.His428Gln
|
|
NM_001281513.2:c.1218C>A
|
NP_001268442.1:p.His406Gln
|
|
NM_001281512.2:c.1239C>A
|
NP_001268441.1:p.His413Gln
|
|