ENST00000298910.12:c.7082C>G
MANE Select
|
ENSP00000298910.7:p.Thr2361Ser
|
|
ENST00000636518.1:c.879C>G
|
|
|
ENST00000679360.1:c.*5991C>G
|
ENSP00000505368.1:n.*5991C>G
|
|
ENST00000679532.1:c.2856C>G
|
|
|
ENST00000679683.1:c.872C>G
|
|
|
ENST00000680018.1:c.2527C>G
|
ENSP00000505347.1:n.2527C>G
|
|
ENST00000680422.1:c.4169C>G
|
|
|
ENST00000680425.1:c.2249C>G
|
ENSP00000506459.1:n.2249C>G
|
|
ENST00000680453.1:c.2539C>G
|
|
|
ENST00000680790.1:c.6827C>G
|
ENSP00000505335.1:p.Thr2276Ser
|
|
ENST00000681136.1:n.3066C>G
|
|
|
ENST00000681696.1:c.2765C>G
|
ENSP00000505871.1:p.Thr922Ser
|
|
ENST00000681773.1:n.289C>G
|
|
|
ENST00000298910.11:c.7082C>G
|
ENSP00000298910.7:p.Thr2361Ser
|
|
ENST00000430804.5:c.4378C>G
|
|
|
ENST00000479187.5:n.3763C>G
|
|
|
NM_198578.3:c.7082C>G
|
NP_940980.3:p.Thr2361Ser
|
|
XM_005268629.2:c.7082C>G
|
XP_005268686.1:p.Thr2361Ser
|
|
XM_011537877.1:c.7082C>G
|
XP_011536179.1:p.Thr2361Ser
|
|
XM_011537879.1:c.5879C>G
|
XP_011536181.1:p.Thr1960Ser
|
|
XR_944868.1:n.485-8628G>C
|
|
|
XM_005268629.4:c.7082C>G
|
XP_005268686.1:p.Thr2361Ser
|
|
XM_011537877.3:c.7082C>G
|
XP_011536179.1:p.Thr2361Ser
|
|
XM_017018787.1:c.3998C>G
|
XP_016874276.1:p.Thr1333Ser
|
|
XM_017018788.2:c.3344C>G
|
XP_016874277.1:p.Thr1115Ser
|
|
XM_024448833.1:c.5879C>G
|
XP_024304601.1:p.Thr1960Ser
|
|
XR_944868.2:n.485-8628G>C
|
|
|
NM_198578.4:c.7082C>G
MANE Select
|
NP_940980.4:p.Thr2361Ser
|
|