ENST00000373588.9:c.915G>C
MANE Select
|
ENSP00000362690.4:p.Leu305=
|
|
ENST00000373587.3:c.267G>C
|
ENSP00000362689.3:p.Leu89=
|
|
ENST00000373588.8:c.915G>C
|
ENSP00000362690.4:p.Leu305=
|
|
ENST00000620110.4:c.871-1877G>C
|
ENSP00000483309.1:n.871-1877G>C
|
|
NM_004959.4:c.915G>C
|
NP_004950.2:p.Leu305=
|
|
XM_005251871.2:c.915G>C
|
XP_005251928.1:p.Leu305=
|
|
XM_005251872.3:c.654G>C
|
XP_005251929.1:p.Leu218=
|
|
XM_011518455.1:c.915G>C
|
XP_011516757.1:p.Leu305=
|
|
XM_011518456.1:c.870+6985G>C
|
XP_011516758.1:n.870+6985G>C
|
|
NM_004959.5:c.915G>C
MANE Select
|
NP_004950.2:p.Leu305=
|
|