ENST00000218099.7:c.591T>G
MANE Select
|
ENSP00000218099.2:p.Pro197=
|
|
ENST00000643157.1:n.1258T>G
|
|
|
ENST00000218099.6:c.591T>G
|
ENSP00000218099.2:p.Pro197=
|
|
ENST00000394090.2:c.477T>G
|
ENSP00000377650.2:p.Pro159=
|
|
NM_000133.3:c.591T>G , LRG_556t1:c.591T>G
|
NP_000124.1:p.Pro197=
|
|
NM_001313913.1:c.477T>G
|
NP_001300842.1:p.Pro159=
|
|
XM_005262397.3:c.462T>G
|
XP_005262454.1:p.Pro154=
|
|
XM_005262397.4:c.462T>G
|
XP_005262454.1:p.Pro154=
|
|
NM_000133.4:c.591T>G
MANE Select
|
NP_000124.1:p.Pro197=
|
|
NM_001313913.2:c.477T>G
|
NP_001300842.1:p.Pro159=
|
|