ENST00000393716.8:c.34G>T
MANE Select
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ENSP00000377319.3:p.Ala12Ser
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ENST00000466380.6:c.34G>T
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ENSP00000420297.2:p.Ala12Ser
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ENST00000648112.1:c.*57G>T
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ENSP00000497876.1:n.*57G>T
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ENST00000337940.4:c.151G>T
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ENSP00000336528.4:p.Ala51Ser
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ENST00000393716.6:c.34G>T
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ENSP00000377319.2:p.Ala12Ser
|
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ENST00000466380.5:c.34G>T
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ENSP00000420297.1:p.Ala12Ser
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ENST00000474090.1:n.322G>T
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|
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NM_003889.3:c.34G>T
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NP_003880.3:p.Ala12Ser
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NM_022002.2:c.151G>T
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NP_071285.1:p.Ala51Ser
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NM_033013.2:c.34G>T
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NP_148934.1:p.Ala12Ser
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|
NM_003889.4:c.34G>T
MANE Select
|
NP_003880.3:p.Ala12Ser
|
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NM_022002.3:c.151G>T
|
NP_071285.1:p.Ala51Ser
|
|
NM_033013.3:c.34G>T
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NP_148934.1:p.Ala12Ser
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