ENST00000409110.6:c.1116T>G
MANE Select
|
ENSP00000386444.1:p.Tyr372Ter
|
|
ENST00000409110.5:c.1116T>G
|
ENSP00000386444.1:p.Tyr372Ter
|
|
ENST00000412969.6:n.2336T>G
|
|
|
ENST00000471884.5:n.3147T>G
|
|
|
ENST00000474220.5:n.322T>G
|
|
|
ENST00000476500.5:n.6415T>G
|
|
|
ENST00000492629.1:n.77T>G
|
|
|
NM_000541.4:c.1116T>G
|
NP_000532.2:p.Tyr372Ter
|
|
XM_011511589.1:c.1116T>G
|
XP_011509891.1:p.Tyr372Ter
|
|
XM_011511590.1:c.1116T>G
|
XP_011509892.1:p.Tyr372Ter
|
|
XM_011511591.1:c.1106T>G
|
XP_011509893.1:p.Ile369Ser
|
|
XM_011511592.1:c.960T>G
|
XP_011509894.1:p.Tyr320Ter
|
|
XM_011511593.1:c.816T>G
|
XP_011509895.1:p.Tyr272Ter
|
|
XM_011511594.1:c.744T>G
|
XP_011509896.1:p.Tyr248Ter
|
|
XM_011511596.1:c.714T>G
|
XP_011509898.1:p.Tyr238Ter
|
|
XM_011511597.1:c.714T>G
|
XP_011509899.1:p.Tyr238Ter
|
|
XR_922978.1:n.1433T>G
|
|
|
XR_922979.1:n.1437T>G
|
|
|
XR_922980.1:n.1532T>G
|
|
|
XM_011511593.3:c.816T>G
|
XP_011509895.1:p.Tyr272Ter
|
|
XM_017004641.1:c.1106T>G
|
XP_016860130.1:p.Ile369Ser
|
|
XM_024453036.1:c.704T>G
|
XP_024308804.1:p.Ile235Ser
|
|
XR_001738882.1:n.1314T>G
|
|
|
XR_922980.2:n.1532T>G
|
|
|
NM_000541.5:c.1116T>G
MANE Select
|
NP_000532.2:p.Tyr372Ter
|
|