ENST00000396373.9:c.1237C>T
MANE Select
|
ENSP00000379658.3:p.Gln413Ter
|
|
ENST00000266427.3:c.74C>T
|
|
|
ENST00000396373.8:c.1237C>T
|
ENSP00000379658.3:p.Gln413Ter
|
|
NM_001987.4:c.1237C>T , LRG_609t1:c.1237C>T
|
NP_001978.1:p.Gln413Ter
|
|
XM_011520607.1:c.1234C>T
|
XP_011518909.1:p.Gln412Ter
|
|
XM_011520608.1:c.1210C>T
|
XP_011518910.1:p.Gln404Ter
|
|
XM_011520609.1:c.973C>T
|
XP_011518911.1:p.Gln325Ter
|
|
XM_011520610.1:c.973C>T
|
XP_011518912.1:p.Gln325Ter
|
|
XM_011520611.1:c.973C>T
|
XP_011518913.1:p.Gln325Ter
|
|
XM_011520612.1:c.616C>T
|
XP_011518914.1:p.Gln206Ter
|
|
XM_011520607.2:c.1234C>T
|
XP_011518909.1:p.Gln412Ter
|
|
XM_011520608.2:c.1210C>T
|
XP_011518910.1:p.Gln404Ter
|
|
XM_011520609.2:c.973C>T
|
XP_011518911.1:p.Gln325Ter
|
|
XM_011520611.2:c.973C>T
|
XP_011518913.1:p.Gln325Ter
|
|
XM_011520612.2:c.616C>T
|
XP_011518914.1:p.Gln206Ter
|
|
XM_017018990.1:c.1102C>T
|
XP_016874479.1:p.Gln368Ter
|
|
XM_017018991.1:c.973C>T
|
XP_016874480.1:p.Gln325Ter
|
|
NM_001987.5:c.1237C>T
MANE Select
|
NP_001978.1:p.Gln413Ter
|
|