ENST00000366672.5:c.726G>A
MANE Select
|
ENSP00000355632.4:p.Ala242=
|
|
ENST00000366672.4:c.726G>A
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ENSP00000355632.4:p.Ala242=
|
|
ENST00000494106.1:n.689G>A
|
|
|
NM_001291866.1:c.612G>A
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NP_001278795.1:p.Ala204=
|
|
NM_004481.4:c.726G>A
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NP_004472.1:p.Ala242=
|
|
XM_011544154.1:c.654G>A
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XP_011542456.1:p.Ala218=
|
|
XM_011544155.1:c.525G>A
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XP_011542457.1:p.Ala175=
|
|
XM_017000963.2:c.726G>A
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XP_016856452.1:p.Ala242=
|
|
XM_017000964.2:c.633G>A
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XP_016856453.1:p.Ala211=
|
|
XM_017000965.1:c.612G>A
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XP_016856454.1:p.Ala204=
|
|
XM_017000966.1:c.525G>A
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XP_016856455.1:p.Ala175=
|
|
NM_004481.5:c.726G>A
MANE Select
|
NP_004472.1:p.Ala242=
|
|
NM_001291866.2:c.612G>A
|
NP_001278795.1:p.Ala204=
|
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