|
ENST00000641284.2:c.1669T>G
|
ENSP00000493088.1:p.Phe557Val
|
|
|
ENST00000646677.2:c.1669T>G
|
ENSP00000496533.1:p.Phe557Val
|
|
|
ENST00000641284.1:c.1669T>G
|
ENSP00000493088.1:p.Phe557Val
|
|
|
ENST00000646677.1:c.1669T>G
|
ENSP00000496533.1:p.Phe557Val
|
|
|
ENST00000647318.2:c.1669T>G
MANE Select
|
ENSP00000495993.1:p.Phe557Val
|
|
|
ENST00000300589.6:c.1750T>G
|
ENSP00000300589.2:p.Phe584Val
|
|
|
NM_001293557.1:c.1669T>G
|
NP_001280486.1:p.Phe557Val
|
|
|
NM_022162.2:c.1750T>G
|
NP_071445.1:p.Phe584Val
|
|
|
XM_005256084.2:c.1669T>G
|
XP_005256141.1:p.Phe557Val
|
|
|
XM_006721242.2:c.1669T>G
|
XP_006721305.1:p.Phe557Val
|
|
|
XM_006721243.2:c.1669T>G
|
XP_006721306.1:p.Phe557Val
|
|
|
XM_011523257.1:c.1246T>G
|
XP_011521559.1:p.Phe416Val
|
|
|
XM_011523258.1:c.1246T>G
|
XP_011521560.1:p.Phe416Val
|
|
|
XM_011523259.1:c.1084T>G
|
XP_011521561.1:p.Phe362Val
|
|
|
XM_011523260.1:c.1669T>G
|
XP_011521562.1:p.Phe557Val
|
|
|
XM_011523261.1:c.1669T>G
|
XP_011521563.1:p.Phe557Val
|
|
|
XR_429725.2:n.1759T>G
|
|
|
|
XR_429726.2:n.1759T>G
|
|
|
|
XR_933387.1:n.1759T>G
|
|
|
|
XM_005256084.4:c.1669T>G
|
XP_005256141.1:p.Phe557Val
|
|
|
XM_006721242.4:c.1669T>G
|
XP_006721305.1:p.Phe557Val
|
|
|
XM_006721243.4:c.1669T>G
|
XP_006721306.1:p.Phe557Val
|
|
|
XM_011523259.2:c.1084T>G
|
XP_011521561.1:p.Phe362Val
|
|
|
XM_011523260.3:c.1669T>G
|
XP_011521562.1:p.Phe557Val
|
|
|
XM_011523261.2:c.1669T>G
|
XP_011521563.1:p.Phe557Val
|
|
|
XM_017023535.1:c.1177T>G
|
XP_016879024.1:p.Phe393Val
|
|
|
XM_017023536.1:c.1084T>G
|
XP_016879025.1:p.Phe362Val
|
|
|
XM_017023537.1:c.1084T>G
|
XP_016879026.1:p.Phe362Val
|
|
|
XM_017023538.1:c.1084T>G
|
XP_016879027.1:p.Phe362Val
|
|
|
XR_429725.3:n.1712T>G
|
|
|
|
XR_429726.3:n.1712T>G
|
|
|
|
XR_933387.2:n.1712T>G
|
|
|
|
NM_001293557.2:c.1669T>G
|
NP_001280486.1:p.Phe557Val
|
|
|
NM_001370466.1:c.1669T>G
MANE Select
|
NP_001357395.1:p.Phe557Val
|
|
|
NM_022162.3:c.1750T>G
|
NP_071445.1:p.Phe584Val
|
|
|
NR_163434.1:n.1734T>G
|
|
|
