ENST00000356392.9:c.1140C>G
MANE Select
|
ENSP00000348757.3:p.Ala380=
|
|
ENST00000356392.8:c.1140C>G
|
ENSP00000348757.3:p.Ala380=
|
|
ENST00000586836.5:c.567C>G
|
ENSP00000467429.1:p.Ala189=
|
|
ENST00000591179.5:c.960C>G
|
ENSP00000466800.1:p.Ala320=
|
|
ENST00000591345.5:c.*1059C>G
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ENSP00000467313.1:n.*1059C>G
|
|
NM_001302453.1:c.978C>G
|
NP_001289382.1:p.Ala326=
|
|
NM_001302454.1:c.960C>G
|
NP_001289383.1:p.Ala320=
|
|
NM_145045.4:c.1140C>G
|
NP_659482.3:p.Ala380=
|
|
XM_017026241.1:c.*34C>G
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XP_016881730.1:n.*34C>G
|
|
NM_145045.5:c.1140C>G
MANE Select
|
NP_659482.3:p.Ala380=
|
|
NM_001302454.2:c.960C>G
|
NP_001289383.1:p.Ala320=
|
|