ENST00000373588.9:c.892C>G
MANE Select
|
ENSP00000362690.4:p.Leu298Val
|
|
ENST00000373587.3:c.244C>G
|
ENSP00000362689.3:p.Leu82Val
|
|
ENST00000373588.8:c.892C>G
|
ENSP00000362690.4:p.Leu298Val
|
|
ENST00000620110.4:c.871-1900C>G
|
ENSP00000483309.1:n.871-1900C>G
|
|
NM_004959.4:c.892C>G
|
NP_004950.2:p.Leu298Val
|
|
XM_005251871.2:c.892C>G
|
XP_005251928.1:p.Leu298Val
|
|
XM_005251872.3:c.631C>G
|
XP_005251929.1:p.Leu211Val
|
|
XM_011518455.1:c.892C>G
|
XP_011516757.1:p.Leu298Val
|
|
XM_011518456.1:c.870+6962C>G
|
XP_011516758.1:n.870+6962C>G
|
|
NM_004959.5:c.892C>G
MANE Select
|
NP_004950.2:p.Leu298Val
|
|