ENST00000367099.4:n.1456G>T
|
|
|
ENST00000471071.2:c.196G>T
|
ENSP00000493073.2:p.Glu66Ter
|
|
ENST00000640756.2:n.261G>T
|
|
|
ENST00000659065.2:c.334G>T
|
ENSP00000499588.1:p.Glu112Ter
|
|
ENST00000659642.2:c.334G>T
|
ENSP00000499509.1:p.Glu112Ter
|
|
ENST00000664374.2:c.334G>T
|
ENSP00000499664.1:p.Glu112Ter
|
|
ENST00000640756.1:n.250G>T
|
|
|
ENST00000659065.1:c.334G>T
|
ENSP00000499588.1:p.Glu112Ter
|
|
ENST00000659642.1:c.334G>T
|
ENSP00000499509.1:p.Glu112Ter
|
|
ENST00000664374.1:c.334G>T
|
ENSP00000499664.1:p.Glu112Ter
|
|
ENST00000423557.1:c.451G>T
MANE Select
|
ENSP00000412237.1:p.Glu151Ter
|
|
ENST00000471071.1:n.366G>T
|
|
|
NM_000572.2:c.451G>T
|
NP_000563.1:p.Glu151Ter
|
|
XM_011509506.1:c.451G>T
|
XP_011507808.1:p.Glu151Ter
|
|
NM_000572.3:c.451G>T
MANE Select
|
NP_000563.1:p.Glu151Ter
|
|
NM_001382624.1:c.196G>T
|
NP_001369553.1:p.Glu66Ter
|
|
NR_168466.1:n.748G>T
|
|
|
NR_168467.1:n.278G>T
|
|
|