ENST00000393716.8:c.26G>A
MANE Select
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ENSP00000377319.3:p.Trp9Ter
|
|
ENST00000466380.6:c.26G>A
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ENSP00000420297.2:p.Trp9Ter
|
|
ENST00000648112.1:c.*49G>A
|
ENSP00000497876.1:n.*49G>A
|
|
ENST00000337940.4:c.143G>A
|
ENSP00000336528.4:p.Trp48Ter
|
|
ENST00000393716.6:c.26G>A
|
ENSP00000377319.2:p.Trp9Ter
|
|
ENST00000466380.5:c.26G>A
|
ENSP00000420297.1:p.Trp9Ter
|
|
ENST00000474090.1:n.314G>A
|
|
|
NM_003889.3:c.26G>A
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NP_003880.3:p.Trp9Ter
|
|
NM_022002.2:c.143G>A
|
NP_071285.1:p.Trp48Ter
|
|
NM_033013.2:c.26G>A
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NP_148934.1:p.Trp9Ter
|
|
NM_003889.4:c.26G>A
MANE Select
|
NP_003880.3:p.Trp9Ter
|
|
NM_022002.3:c.143G>A
|
NP_071285.1:p.Trp48Ter
|
|
NM_033013.3:c.26G>A
|
NP_148934.1:p.Trp9Ter
|
|