ENST00000321612.8:c.2099C>G
MANE Select
|
ENSP00000370737.4:p.Pro700Arg
|
|
ENST00000638233.1:n.534C>G
|
|
|
ENST00000638661.1:c.299C>G
|
ENSP00000491369.1:p.Pro100Arg
|
|
ENST00000638694.1:n.286C>G
|
|
|
ENST00000639318.1:c.299C>G
|
ENSP00000491932.1:p.Pro100Arg
|
|
ENST00000639364.1:n.1799C>G
|
|
|
ENST00000639443.1:n.1667C>G
|
|
|
ENST00000639954.1:n.1807C>G
|
|
|
ENST00000640505.1:n.338C>G
|
|
|
ENST00000321612.6:c.2099C>G
|
ENSP00000370737.3:p.Pro700Arg
|
|
NM_000170.2:c.2099C>G , LRG_643t1:c.2099C>G
|
NP_000161.2:p.Pro700Arg
|
|
NM_000170.3:c.2099C>G
MANE Select
|
NP_000161.2:p.Pro700Arg
|
|