ENST00000298910.12:c.7054T>A
MANE Select
|
ENSP00000298910.7:p.Ser2352Thr
|
|
ENST00000636518.1:c.851T>A
|
|
|
ENST00000679360.1:c.*5963T>A
|
ENSP00000505368.1:n.*5963T>A
|
|
ENST00000679532.1:c.2828T>A
|
|
|
ENST00000679683.1:c.844T>A
|
|
|
ENST00000680018.1:c.2499T>A
|
ENSP00000505347.1:n.2499T>A
|
|
ENST00000680422.1:c.4141T>A
|
|
|
ENST00000680425.1:c.2221T>A
|
ENSP00000506459.1:n.2221T>A
|
|
ENST00000680453.1:c.2511T>A
|
|
|
ENST00000680790.1:c.6799T>A
|
ENSP00000505335.1:p.Ser2267Thr
|
|
ENST00000681136.1:n.3038T>A
|
|
|
ENST00000681696.1:c.2737T>A
|
ENSP00000505871.1:p.Ser913Thr
|
|
ENST00000681773.1:n.261T>A
|
|
|
ENST00000298910.11:c.7054T>A
|
ENSP00000298910.7:p.Ser2352Thr
|
|
ENST00000430804.5:c.4350T>A
|
|
|
ENST00000479187.5:n.3735T>A
|
|
|
NM_198578.3:c.7054T>A
|
NP_940980.3:p.Ser2352Thr
|
|
XM_005268629.2:c.7054T>A
|
XP_005268686.1:p.Ser2352Thr
|
|
XM_011537877.1:c.7054T>A
|
XP_011536179.1:p.Ser2352Thr
|
|
XM_011537879.1:c.5851T>A
|
XP_011536181.1:p.Ser1951Thr
|
|
XR_944868.1:n.485-8600A>T
|
|
|
XM_005268629.4:c.7054T>A
|
XP_005268686.1:p.Ser2352Thr
|
|
XM_011537877.3:c.7054T>A
|
XP_011536179.1:p.Ser2352Thr
|
|
XM_017018787.1:c.3970T>A
|
XP_016874276.1:p.Ser1324Thr
|
|
XM_017018788.2:c.3316T>A
|
XP_016874277.1:p.Ser1106Thr
|
|
XM_024448833.1:c.5851T>A
|
XP_024304601.1:p.Ser1951Thr
|
|
XR_944868.2:n.485-8600A>T
|
|
|
NM_198578.4:c.7054T>A
MANE Select
|
NP_940980.4:p.Ser2352Thr
|
|