ENST00000298910.12:c.5975A>G
MANE Select
|
ENSP00000298910.7:p.Tyr1992Cys
|
|
ENST00000679360.1:c.*4884A>G
|
ENSP00000505368.1:n.*4884A>G
|
|
ENST00000679532.1:c.1749A>G
|
|
|
ENST00000680018.1:c.1420A>G
|
ENSP00000505347.1:n.1420A>G
|
|
ENST00000680422.1:c.1620A>G
|
|
|
ENST00000680425.1:c.1142A>G
|
ENSP00000506459.1:n.1142A>G
|
|
ENST00000680453.1:c.1432A>G
|
|
|
ENST00000680790.1:c.5720A>G
|
ENSP00000505335.1:p.Tyr1907Cys
|
|
ENST00000681136.1:n.1959A>G
|
|
|
ENST00000681696.1:c.1658A>G
|
ENSP00000505871.1:p.Tyr553Cys
|
|
ENST00000298910.11:c.5975A>G
|
ENSP00000298910.7:p.Tyr1992Cys
|
|
ENST00000430804.5:c.3271A>G
|
|
|
ENST00000479187.5:n.2656A>G
|
|
|
NM_198578.3:c.5975A>G
|
NP_940980.3:p.Tyr1992Cys
|
|
XM_005268629.2:c.5975A>G
|
XP_005268686.1:p.Tyr1992Cys
|
|
XM_011537877.1:c.5975A>G
|
XP_011536179.1:p.Tyr1992Cys
|
|
XM_011537878.1:c.5975A>G
|
XP_011536180.1:p.Tyr1992Cys
|
|
XM_011537879.1:c.4772A>G
|
XP_011536181.1:p.Tyr1591Cys
|
|
XM_005268629.4:c.5975A>G
|
XP_005268686.1:p.Tyr1992Cys
|
|
XM_011537877.3:c.5975A>G
|
XP_011536179.1:p.Tyr1992Cys
|
|
XM_017018787.1:c.2891A>G
|
XP_016874276.1:p.Tyr964Cys
|
|
XM_017018788.2:c.2237A>G
|
XP_016874277.1:p.Tyr746Cys
|
|
XM_024448833.1:c.4772A>G
|
XP_024304601.1:p.Tyr1591Cys
|
|
NM_198578.4:c.5975A>G
MANE Select
|
NP_940980.4:p.Tyr1992Cys
|
|