ENST00000400723.8:c.163+92C>G
MANE Select
|
ENSP00000383558.3:n.163+92C>G
|
|
ENST00000400723.7:c.163+92C>G
|
ENSP00000383558.3:n.163+92C>G
|
|
ENST00000570996.5:c.163+92C>G
|
ENSP00000460976.1:n.163+92C>G
|
|
ENST00000572185.1:n.550C>G
|
|
|
ENST00000573428.1:c.163+92C>G
|
ENSP00000458930.1:n.163+92C>G
|
|
ENST00000574283.2:n.189C>G
|
|
|
NM_000160.4:c.163+92C>G
|
NP_000151.1:n.163+92C>G
|
|
XM_006722277.1:c.163+92C>G
|
XP_006722340.1:n.163+92C>G
|
|
XM_011523539.1:c.29C>G
|
XP_011521841.1:p.Ala10Gly
|
|
XM_011523540.1:c.-262C>G
|
XP_011521842.1:n.-262C>G
|
|
XM_017024446.1:c.157+92C>G
|
XP_016879935.1:n.157+92C>G
|
|
XM_017024447.1:c.-262C>G
|
XP_016879936.1:n.-262C>G
|
|
NM_000160.5:c.163+92C>G
MANE Select
|
NP_000151.1:n.163+92C>G
|
|