ENST00000298910.12:c.6426A>T
MANE Select
|
ENSP00000298910.7:p.Arg2142Ser
|
|
ENST00000636518.1:c.223A>T
|
|
|
ENST00000679360.1:c.*5335A>T
|
ENSP00000505368.1:n.*5335A>T
|
|
ENST00000679532.1:c.2200A>T
|
|
|
ENST00000679683.1:c.216A>T
|
|
|
ENST00000680018.1:c.1871A>T
|
ENSP00000505347.1:n.1871A>T
|
|
ENST00000680422.1:c.2071A>T
|
|
|
ENST00000680425.1:c.1593A>T
|
ENSP00000506459.1:n.1593A>T
|
|
ENST00000680453.1:c.1883A>T
|
|
|
ENST00000680790.1:c.6171A>T
|
ENSP00000505335.1:p.Arg2057Ser
|
|
ENST00000681136.1:n.2410A>T
|
|
|
ENST00000681696.1:c.2109A>T
|
ENSP00000505871.1:p.Arg703Ser
|
|
ENST00000298910.11:c.6426A>T
|
ENSP00000298910.7:p.Arg2142Ser
|
|
ENST00000430804.5:c.3722A>T
|
|
|
ENST00000479187.5:n.3107A>T
|
|
|
NM_198578.3:c.6426A>T
|
NP_940980.3:p.Arg2142Ser
|
|
XM_005268629.2:c.6426A>T
|
XP_005268686.1:p.Arg2142Ser
|
|
XM_011537877.1:c.6426A>T
|
XP_011536179.1:p.Arg2142Ser
|
|
XM_011537878.1:c.6426A>T
|
XP_011536180.1:p.Arg2142Ser
|
|
XM_011537879.1:c.5223A>T
|
XP_011536181.1:p.Arg1741Ser
|
|
XM_005268629.4:c.6426A>T
|
XP_005268686.1:p.Arg2142Ser
|
|
XM_011537877.3:c.6426A>T
|
XP_011536179.1:p.Arg2142Ser
|
|
XM_017018787.1:c.3342A>T
|
XP_016874276.1:p.Arg1114Ser
|
|
XM_017018788.2:c.2688A>T
|
XP_016874277.1:p.Arg896Ser
|
|
XM_024448833.1:c.5223A>T
|
XP_024304601.1:p.Arg1741Ser
|
|
NM_198578.4:c.6426A>T
MANE Select
|
NP_940980.4:p.Arg2142Ser
|
|