ENST00000651671.1:c.6510C>T
MANE Select
|
ENSP00000498587.1:p.Ser2170=
|
|
ENST00000679595.1:c.*1550C>T
|
ENSP00000506241.1:n.*1550C>T
|
|
ENST00000679969.1:n.3106C>T
|
|
|
ENST00000680003.1:n.2842C>T
|
|
|
ENST00000680133.1:c.6396C>T
|
ENSP00000505319.1:p.Ser2132=
|
|
ENST00000680218.1:c.6390C>T
|
ENSP00000505339.1:p.Ser2130=
|
|
ENST00000680668.1:c.6396C>T
|
ENSP00000506336.1:p.Ser2132=
|
|
ENST00000680778.1:c.4107C>T
|
ENSP00000506033.1:p.Ser1369=
|
|
ENST00000680924.1:c.*3910C>T
|
ENSP00000506031.1:n.*3910C>T
|
|
ENST00000681135.1:c.*4119C>T
|
ENSP00000506636.1:n.*4119C>T
|
|
ENST00000681298.1:n.4615C>T
|
|
|
ENST00000681454.1:c.*5746C>T
|
ENSP00000505763.1:n.*5746C>T
|
|
ENST00000277541.6:c.6510C>T
|
ENSP00000277541.6:p.Ser2170=
|
|
NM_017617.3:c.6510C>T
|
NP_060087.3:p.Ser2170=
|
|
XM_011518717.1:c.5811C>T
|
XP_011517019.1:p.Ser1937=
|
|
NM_017617.5:c.6510C>T
MANE Select
|
NP_060087.3:p.Ser2170=
|
|
XM_011518717.2:c.5787C>T
|
XP_011517019.2:p.Ser1929=
|
|