ENST00000321612.8:c.1997A>C
MANE Select
|
ENSP00000370737.4:p.Gln666Pro
|
|
ENST00000460457.2:n.157A>C
|
|
|
ENST00000638233.1:n.432A>C
|
|
|
ENST00000638661.1:c.197A>C
|
ENSP00000491369.1:p.Gln66Pro
|
|
ENST00000638694.1:n.184A>C
|
|
|
ENST00000639318.1:c.197A>C
|
ENSP00000491932.1:p.Gln66Pro
|
|
ENST00000639364.1:n.1697A>C
|
|
|
ENST00000639443.1:n.1565A>C
|
|
|
ENST00000639954.1:n.1705A>C
|
|
|
ENST00000640208.1:c.197A>C
|
ENSP00000491895.1:p.Gln66Pro
|
|
ENST00000640505.1:n.236A>C
|
|
|
ENST00000640592.1:n.1880A>C
|
|
|
ENST00000321612.6:c.1997A>C
|
ENSP00000370737.3:p.Gln666Pro
|
|
ENST00000460457.1:n.136A>C
|
|
|
NM_000170.2:c.1997A>C , LRG_643t1:c.1997A>C
|
NP_000161.2:p.Gln666Pro
|
|
NM_000170.3:c.1997A>C
MANE Select
|
NP_000161.2:p.Gln666Pro
|
|