ENST00000373588.9:c.990+12C>G
MANE Select
|
ENSP00000362690.4:n.990+12C>G
|
|
ENST00000373587.3:c.342+12C>G
|
ENSP00000362689.3:n.342+12C>G
|
|
ENST00000373588.8:c.990+12C>G
|
ENSP00000362690.4:n.990+12C>G
|
|
ENST00000620110.4:c.871-1790C>G
|
ENSP00000483309.1:n.871-1790C>G
|
|
NM_004959.4:c.990+12C>G
|
NP_004950.2:n.990+12C>G
|
|
XM_005251871.2:c.990+12C>G
|
XP_005251928.1:n.990+12C>G
|
|
XM_005251872.3:c.729+12C>G
|
XP_005251929.1:n.729+12C>G
|
|
XM_011518455.1:c.990+12C>G
|
XP_011516757.1:n.990+12C>G
|
|
XM_011518456.1:c.870+7072C>G
|
XP_011516758.1:n.870+7072C>G
|
|
NM_004959.5:c.990+12C>G
MANE Select
|
NP_004950.2:n.990+12C>G
|
|