ENST00000218099.7:c.971C>G
MANE Select
|
ENSP00000218099.2:p.Pro324Arg
|
|
ENST00000643157.1:n.1638C>G
|
|
|
ENST00000218099.6:c.971C>G
|
ENSP00000218099.2:p.Pro324Arg
|
|
ENST00000394090.2:c.857C>G
|
ENSP00000377650.2:p.Pro286Arg
|
|
NM_000133.3:c.971C>G , LRG_556t1:c.971C>G
|
NP_000124.1:p.Pro324Arg
|
|
NM_001313913.1:c.857C>G
|
NP_001300842.1:p.Pro286Arg
|
|
XM_005262397.3:c.842C>G
|
XP_005262454.1:p.Pro281Arg
|
|
XM_005262397.4:c.842C>G
|
XP_005262454.1:p.Pro281Arg
|
|
NM_000133.4:c.971C>G
MANE Select
|
NP_000124.1:p.Pro324Arg
|
|
NM_001313913.2:c.857C>G
|
NP_001300842.1:p.Pro286Arg
|
|