ENST00000298910.12:c.6401C>G
MANE Select
|
ENSP00000298910.7:p.Ser2134Ter
|
|
ENST00000636518.1:c.198C>G
|
|
|
ENST00000679360.1:c.*5310C>G
|
ENSP00000505368.1:n.*5310C>G
|
|
ENST00000679532.1:c.2175C>G
|
|
|
ENST00000679683.1:c.191C>G
|
|
|
ENST00000680018.1:c.1846C>G
|
ENSP00000505347.1:n.1846C>G
|
|
ENST00000680422.1:c.2046C>G
|
|
|
ENST00000680425.1:c.1568C>G
|
ENSP00000506459.1:n.1568C>G
|
|
ENST00000680453.1:c.1858C>G
|
|
|
ENST00000680790.1:c.6146C>G
|
ENSP00000505335.1:p.Ser2049Ter
|
|
ENST00000681136.1:n.2385C>G
|
|
|
ENST00000681696.1:c.2084C>G
|
ENSP00000505871.1:p.Ser695Ter
|
|
ENST00000298910.11:c.6401C>G
|
ENSP00000298910.7:p.Ser2134Ter
|
|
ENST00000430804.5:c.3697C>G
|
|
|
ENST00000479187.5:n.3082C>G
|
|
|
NM_198578.3:c.6401C>G
|
NP_940980.3:p.Ser2134Ter
|
|
XM_005268629.2:c.6401C>G
|
XP_005268686.1:p.Ser2134Ter
|
|
XM_011537877.1:c.6401C>G
|
XP_011536179.1:p.Ser2134Ter
|
|
XM_011537878.1:c.6401C>G
|
XP_011536180.1:p.Ser2134Ter
|
|
XM_011537879.1:c.5198C>G
|
XP_011536181.1:p.Ser1733Ter
|
|
XM_005268629.4:c.6401C>G
|
XP_005268686.1:p.Ser2134Ter
|
|
XM_011537877.3:c.6401C>G
|
XP_011536179.1:p.Ser2134Ter
|
|
XM_017018787.1:c.3317C>G
|
XP_016874276.1:p.Ser1106Ter
|
|
XM_017018788.2:c.2663C>G
|
XP_016874277.1:p.Ser888Ter
|
|
XM_024448833.1:c.5198C>G
|
XP_024304601.1:p.Ser1733Ter
|
|
NM_198578.4:c.6401C>G
MANE Select
|
NP_940980.4:p.Ser2134Ter
|
|