|
ENST00000647165.2:c.6276C>A
MANE Select
|
ENSP00000495481.1:p.Ile2092=
|
|
|
ENST00000205890.9:c.6276C>A
|
ENSP00000205890.5:p.Ile2092=
|
|
|
ENST00000615845.4:c.6276C>A
|
ENSP00000481642.1:p.Ile2092=
|
|
|
NM_016239.3:c.6276C>A
|
NP_057323.3:p.Ile2092=
|
|
|
XM_011523917.1:c.6216C>A
|
XP_011522219.1:p.Ile2072=
|
|
|
XM_011523918.1:c.6216C>A
|
XP_011522220.1:p.Ile2072=
|
|
|
XM_011523921.1:c.6270C>A
|
XP_011522223.1:p.Ile2090=
|
|
|
XR_934037.1:n.6875C>A
|
|
|
|
XR_934038.1:n.6875C>A
|
|
|
|
XM_011523918.2:c.6216C>A
|
XP_011522220.1:p.Ile2072=
|
|
|
XM_017024714.2:c.6216C>A
|
XP_016880203.1:p.Ile2072=
|
|
|
XM_017024715.2:c.6279C>A
|
XP_016880204.1:p.Ile2093=
|
|
|
XM_024450781.1:c.6213+1282C>A
|
XP_024306549.1:n.6213+1282C>A
|
|
|
NM_016239.4:c.6276C>A
MANE Select
|
NP_057323.3:p.Ile2092=
|
|
