ENST00000344327.8:c.1773T>G
MANE Select
|
ENSP00000340913.3:p.Pro591=
|
|
ENST00000344327.7:c.1773T>G
|
ENSP00000340913.3:p.Pro591=
|
|
ENST00000348423.8:c.1425T>G
|
ENSP00000343672.4:p.Pro475=
|
|
ENST00000360497.4:c.1608T>G
|
ENSP00000353687.4:p.Pro536=
|
|
ENST00000532133.5:c.1539T>G
|
ENSP00000435574.1:p.Pro513=
|
|
NM_004621.5:c.1773T>G
|
NP_004612.2:p.Pro591=
|
|
XM_006718898.2:c.1773T>G
|
XP_006718961.1:p.Pro591=
|
|
XM_011542968.1:c.1608T>G
|
XP_011541270.1:p.Pro536=
|
|
XM_011542969.1:c.1773T>G
|
XP_011541271.1:p.Pro591=
|
|
XM_011542968.3:c.1608T>G
|
XP_011541270.1:p.Pro536=
|
|
XM_017018221.2:c.1425T>G
|
XP_016873710.1:p.Pro475=
|
|
XR_001747948.2:n.2129T>G
|
|
|
NM_004621.6:c.1773T>G
MANE Select
|
NP_004612.2:p.Pro591=
|
|