ENST00000304611.13:c.1358T>G
MANE Select
|
ENSP00000303511.8:p.Leu453Arg
|
|
ENST00000244546.4:c.1358T>G
|
ENSP00000244546.4:p.Leu453Arg
|
|
ENST00000304611.12:c.1358T>G
|
ENSP00000303511.8:p.Leu453Arg
|
|
NM_000287.3:c.1358T>G
|
NP_000278.3:p.Leu453Arg
|
|
NM_001316313.1:c.1094T>G
|
NP_001303242.1:p.Leu365Arg
|
|
NR_133009.1:n.1451T>G
|
|
|
XM_011514661.1:c.1274T>G
|
XP_011512963.1:p.Leu425Arg
|
|
XR_926246.1:n.1451T>G
|
|
|
XM_011514661.2:c.1274T>G
|
XP_011512963.1:p.Leu425Arg
|
|
XR_001743466.2:n.2432T>G
|
|
|
NM_000287.4:c.1358T>G
MANE Select
|
NP_000278.3:p.Leu453Arg
|
|
NM_001316313.2:c.1094T>G
|
NP_001303242.1:p.Leu365Arg
|
|
NR_133009.2:n.1389T>G
|
|
|