ENST00000298910.12:c.7066A>T
MANE Select
|
ENSP00000298910.7:p.Thr2356Ser
|
|
ENST00000636518.1:c.863A>T
|
|
|
ENST00000679360.1:c.*5975A>T
|
ENSP00000505368.1:n.*5975A>T
|
|
ENST00000679532.1:c.2840A>T
|
|
|
ENST00000679683.1:c.856A>T
|
|
|
ENST00000680018.1:c.2511A>T
|
ENSP00000505347.1:n.2511A>T
|
|
ENST00000680422.1:c.4153A>T
|
|
|
ENST00000680425.1:c.2233A>T
|
ENSP00000506459.1:n.2233A>T
|
|
ENST00000680453.1:c.2523A>T
|
|
|
ENST00000680790.1:c.6811A>T
|
ENSP00000505335.1:p.Thr2271Ser
|
|
ENST00000681136.1:n.3050A>T
|
|
|
ENST00000681696.1:c.2749A>T
|
ENSP00000505871.1:p.Thr917Ser
|
|
ENST00000681773.1:n.273A>T
|
|
|
ENST00000298910.11:c.7066A>T
|
ENSP00000298910.7:p.Thr2356Ser
|
|
ENST00000430804.5:c.4362A>T
|
|
|
ENST00000479187.5:n.3747A>T
|
|
|
NM_198578.3:c.7066A>T
|
NP_940980.3:p.Thr2356Ser
|
|
XM_005268629.2:c.7066A>T
|
XP_005268686.1:p.Thr2356Ser
|
|
XM_011537877.1:c.7066A>T
|
XP_011536179.1:p.Thr2356Ser
|
|
XM_011537879.1:c.5863A>T
|
XP_011536181.1:p.Thr1955Ser
|
|
XR_944868.1:n.485-8612T>A
|
|
|
XM_005268629.4:c.7066A>T
|
XP_005268686.1:p.Thr2356Ser
|
|
XM_011537877.3:c.7066A>T
|
XP_011536179.1:p.Thr2356Ser
|
|
XM_017018787.1:c.3982A>T
|
XP_016874276.1:p.Thr1328Ser
|
|
XM_017018788.2:c.3328A>T
|
XP_016874277.1:p.Thr1110Ser
|
|
XM_024448833.1:c.5863A>T
|
XP_024304601.1:p.Thr1955Ser
|
|
XR_944868.2:n.485-8612T>A
|
|
|
NM_198578.4:c.7066A>T
MANE Select
|
NP_940980.4:p.Thr2356Ser
|
|