ENST00000261208.8:c.738A>G
MANE Select
|
ENSP00000261208.3:p.Pro246=
|
|
ENST00000261208.7:c.738A>G
|
ENSP00000261208.3:p.Pro246=
|
|
ENST00000538703.5:c.738A>G
|
ENSP00000440861.1:p.Pro246=
|
|
ENST00000541929.5:c.114A>G
|
ENSP00000446364.1:p.Pro38=
|
|
ENST00000544080.6:c.*167A>G
|
ENSP00000439385.2:n.*167A>G
|
|
ENST00000546579.1:c.468A>G
|
ENSP00000447543.1:p.Pro156=
|
|
ENST00000546999.5:c.*167A>G
|
ENSP00000447675.1:n.*167A>G
|
|
ENST00000549376.1:n.131A>G
|
|
|
ENST00000552509.5:c.702A>G
|
ENSP00000450372.1:p.Pro234=
|
|
NM_001258333.1:c.114A>G
|
NP_001245262.1:p.Pro38=
|
|
NM_001258334.1:c.738A>G
|
NP_001245263.1:p.Pro246=
|
|
NM_002108.3:c.738A>G
|
NP_002099.1:p.Pro246=
|
|
XM_011538249.1:c.3+2170A>G
|
XP_011536551.1:n.3+2170A>G
|
|
XM_011538249.2:c.3+2170A>G
|
XP_011536551.1:n.3+2170A>G
|
|
NM_002108.4:c.738A>G
MANE Select
|
NP_002099.1:p.Pro246=
|
|
NM_001258334.2:c.738A>G
|
NP_001245263.1:p.Pro246=
|
|
NM_001258333.2:c.114A>G
|
NP_001245262.1:p.Pro38=
|
|