ENST00000356392.9:c.1157C=
MANE Select
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ENSP00000348757.3:p.Ala386=
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|
ENST00000356392.8:c.1157C=
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ENSP00000348757.3:p.Ala386=
|
|
ENST00000586836.5:c.584C=
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ENSP00000467429.1:p.Ala195=
|
|
ENST00000591179.5:c.977C=
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ENSP00000466800.1:p.Ala326=
|
|
ENST00000591345.5:c.*1076C=
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ENSP00000467313.1:n.*1076C=
|
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NM_001302453.1:c.995C=
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NP_001289382.1:p.Ala332=
|
|
NM_001302454.1:c.977C=
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NP_001289383.1:p.Ala326=
|
|
NM_145045.4:c.1157C=
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NP_659482.3:p.Ala386=
|
|
XM_017026241.1:c.*51C=
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XP_016881730.1:n.*51C=
|
|
NM_145045.5:c.1157C=
MANE Select
|
NP_659482.3:p.Ala386=
|
|
NM_001302454.2:c.977C=
|
NP_001289383.1:p.Ala326=
|
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