ENST00000651671.1:c.6540G>T
MANE Select
|
ENSP00000498587.1:p.Arg2180Ser
|
|
ENST00000679595.1:c.*1580G>T
|
ENSP00000506241.1:n.*1580G>T
|
|
ENST00000679969.1:n.3136G>T
|
|
|
ENST00000680003.1:n.2872G>T
|
|
|
ENST00000680133.1:c.6426G>T
|
ENSP00000505319.1:p.Arg2142Ser
|
|
ENST00000680218.1:c.6420G>T
|
ENSP00000505339.1:p.Arg2140Ser
|
|
ENST00000680668.1:c.6426G>T
|
ENSP00000506336.1:p.Arg2142Ser
|
|
ENST00000680778.1:c.4137G>T
|
ENSP00000506033.1:p.Arg1379Ser
|
|
ENST00000680924.1:c.*3940G>T
|
ENSP00000506031.1:n.*3940G>T
|
|
ENST00000681135.1:c.*4149G>T
|
ENSP00000506636.1:n.*4149G>T
|
|
ENST00000681298.1:n.4645G>T
|
|
|
ENST00000681454.1:c.*5776G>T
|
ENSP00000505763.1:n.*5776G>T
|
|
ENST00000277541.6:c.6540G>T
|
ENSP00000277541.6:p.Arg2180Ser
|
|
NM_017617.3:c.6540G>T
|
NP_060087.3:p.Arg2180Ser
|
|
XM_011518717.1:c.5841G>T
|
XP_011517019.1:p.Arg1947Ser
|
|
NM_017617.5:c.6540G>T
MANE Select
|
NP_060087.3:p.Arg2180Ser
|
|
XM_011518717.2:c.5817G>T
|
XP_011517019.2:p.Arg1939Ser
|
|