ENST00000393716.8:c.-16A>G
MANE Select
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ENSP00000377319.3:n.-16A>G
|
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ENST00000466380.6:c.-16A>G
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ENSP00000420297.2:n.-16A>G
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ENST00000648112.1:c.*8A>G
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ENSP00000497876.1:n.*8A>G
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ENST00000337940.4:c.102A>G
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ENSP00000336528.4:p.Arg34=
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|
ENST00000393716.6:c.-16A>G
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ENSP00000377319.2:n.-16A>G
|
|
ENST00000466380.5:c.-16A>G
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ENSP00000420297.1:n.-16A>G
|
|
ENST00000474090.1:n.273A>G
|
|
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NM_003889.3:c.-16A>G
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NP_003880.3:n.-16A>G
|
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NM_022002.2:c.102A>G
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NP_071285.1:p.Arg34=
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|
NM_033013.2:c.-16A>G
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NP_148934.1:n.-16A>G
|
|
NM_003889.4:c.-16A>G
MANE Select
|
NP_003880.3:n.-16A>G
|
|
NM_022002.3:c.102A>G
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NP_071285.1:p.Arg34=
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|
NM_033013.3:c.-16A>G
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NP_148934.1:n.-16A>G
|
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