ENST00000298910.12:c.5020T>A
MANE Select
|
ENSP00000298910.7:p.Ser1674Thr
|
|
ENST00000679360.1:c.*3929T>A
|
ENSP00000505368.1:n.*3929T>A
|
|
ENST00000679532.1:c.794T>A
|
|
|
ENST00000680018.1:c.465T>A
|
ENSP00000505347.1:n.465T>A
|
|
ENST00000680422.1:c.665T>A
|
|
|
ENST00000680425.1:c.187T>A
|
ENSP00000506459.1:n.187T>A
|
|
ENST00000680453.1:c.477T>A
|
|
|
ENST00000680790.1:c.4765T>A
|
ENSP00000505335.1:p.Ser1589Thr
|
|
ENST00000681136.1:n.1004T>A
|
|
|
ENST00000681696.1:c.703T>A
|
ENSP00000505871.1:p.Ser235Thr
|
|
ENST00000298910.11:c.5020T>A
|
ENSP00000298910.7:p.Ser1674Thr
|
|
ENST00000430804.5:c.2316T>A
|
|
|
ENST00000479187.5:n.1701T>A
|
|
|
NM_198578.3:c.5020T>A
|
NP_940980.3:p.Ser1674Thr
|
|
XM_005268629.2:c.5020T>A
|
XP_005268686.1:p.Ser1674Thr
|
|
XM_011537877.1:c.5020T>A
|
XP_011536179.1:p.Ser1674Thr
|
|
XM_011537878.1:c.5020T>A
|
XP_011536180.1:p.Ser1674Thr
|
|
XM_011537879.1:c.3817T>A
|
XP_011536181.1:p.Ser1273Thr
|
|
XM_011537881.1:c.4832T>A
|
XP_011536183.1:p.Val1611Asp
|
|
XM_005268629.4:c.5020T>A
|
XP_005268686.1:p.Ser1674Thr
|
|
XM_011537877.3:c.5020T>A
|
XP_011536179.1:p.Ser1674Thr
|
|
XM_011537881.3:c.4832T>A
|
XP_011536183.1:p.Val1611Asp
|
|
XM_017018787.1:c.1936T>A
|
XP_016874276.1:p.Ser646Thr
|
|
XM_017018788.2:c.1282T>A
|
XP_016874277.1:p.Ser428Thr
|
|
XM_024448833.1:c.3817T>A
|
XP_024304601.1:p.Ser1273Thr
|
|
XR_001748574.2:n.5388T>A
|
|
|
NM_198578.4:c.5020T>A
MANE Select
|
NP_940980.4:p.Ser1674Thr
|
|