ENST00000456935.7:c.1136C>G
MANE Select
|
ENSP00000395473.2:p.Pro379Arg
|
|
ENST00000221363.8:c.1133C>G
|
ENSP00000221363.4:p.Pro378Arg
|
|
ENST00000456935.6:c.1136C>G
|
ENSP00000395473.2:p.Pro379Arg
|
|
ENST00000465830.1:n.300C>G
|
|
|
ENST00000466794.5:n.1035C>G
|
|
|
ENST00000495617.1:n.280+413C>G
|
|
|
NM_000528.3:c.1136C>G
|
NP_000519.2:p.Pro379Arg
|
|
NM_001173498.1:c.1133C>G
|
NP_001166969.1:p.Pro378Arg
|
|
XM_005259913.1:c.1139C>G
|
XP_005259970.1:p.Pro380Arg
|
|
XM_011528017.1:c.35C>G
|
XP_011526319.1:p.Pro12Arg
|
|
XM_005259913.2:c.1139C>G
|
XP_005259970.1:p.Pro380Arg
|
|
XM_024451518.1:c.35C>G
|
XP_024307286.1:p.Pro12Arg
|
|
NM_000528.4:c.1136C>G
MANE Select
|
NP_000519.2:p.Pro379Arg
|
|
NM_001173498.2:c.1133C>G
|
NP_001166969.1:p.Pro378Arg
|
|