ENST00000393716.8:c.50G>T
MANE Select
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ENSP00000377319.3:p.Cys17Phe
|
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ENST00000466380.6:c.50G>T
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ENSP00000420297.2:p.Cys17Phe
|
|
ENST00000648112.1:c.*73G>T
|
ENSP00000497876.1:n.*73G>T
|
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ENST00000337940.4:c.167G>T
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ENSP00000336528.4:p.Cys56Phe
|
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ENST00000393716.6:c.50G>T
|
ENSP00000377319.2:p.Cys17Phe
|
|
ENST00000466380.5:c.50G>T
|
ENSP00000420297.1:p.Cys17Phe
|
|
ENST00000474090.1:n.338G>T
|
|
|
NM_003889.3:c.50G>T
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NP_003880.3:p.Cys17Phe
|
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NM_022002.2:c.167G>T
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NP_071285.1:p.Cys56Phe
|
|
NM_033013.2:c.50G>T
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NP_148934.1:p.Cys17Phe
|
|
NM_003889.4:c.50G>T
MANE Select
|
NP_003880.3:p.Cys17Phe
|
|
NM_022002.3:c.167G>T
|
NP_071285.1:p.Cys56Phe
|
|
NM_033013.3:c.50G>T
|
NP_148934.1:p.Cys17Phe
|
|