NM_005819.6:c.733C>G
MANE Select
|
NP_005810.1:p.Leu245Val
|
ENST00000258301.6:c.733C>G
MANE Select
|
ENSP00000258301.5:p.Leu245Val
|
NM_001286210.1:c.430C>G
|
NP_001273139.1:p.Leu144Val
|
NM_001286210.2:c.430C>G
|
NP_001273139.1:p.Leu144Val
|
NM_005819.5:c.733C>G
|
NP_005810.1:p.Leu245Val
|
ENST00000258301.5:c.733C>G
|
ENSP00000258301.5:p.Leu245Val
|
ENST00000469135.1:n.1276C>G
|
|
ENST00000542060.5:c.430C>G
|
ENSP00000440188.1:p.Leu144Val
|
XM_011509058.1:c.691+8072C>G
|
XP_011507360.1:n.691+8072C>G
|
XM_011509059.1:c.388+8072C>G
|
XP_011507361.1:n.388+8072C>G
|
XM_017000007.1:c.430C>G
|
XP_016855496.1:p.Leu144Val
|