ENST00000321612.8:c.2114T>C
MANE Select
|
ENSP00000370737.4:p.Val705Ala
|
|
ENST00000638233.1:n.549T>C
|
|
|
ENST00000638661.1:c.314T>C
|
ENSP00000491369.1:p.Val105Ala
|
|
ENST00000638694.1:n.301T>C
|
|
|
ENST00000639318.1:c.314T>C
|
ENSP00000491932.1:p.Val105Ala
|
|
ENST00000639364.1:n.1814T>C
|
|
|
ENST00000639443.1:n.1682T>C
|
|
|
ENST00000639954.1:n.1822T>C
|
|
|
ENST00000640505.1:n.353T>C
|
|
|
ENST00000321612.6:c.2114T>C
|
ENSP00000370737.3:p.Val705Ala
|
|
NM_000170.2:c.2114T>C , LRG_643t1:c.2114T>C
|
NP_000161.2:p.Val705Ala
|
|
NM_000170.3:c.2114T>C
MANE Select
|
NP_000161.2:p.Val705Ala
|
|