ENST00000396373.9:c.1231C>T
MANE Select
|
ENSP00000379658.3:p.Pro411Ser
|
|
ENST00000266427.3:c.68C>T
|
|
|
ENST00000396373.8:c.1231C>T
|
ENSP00000379658.3:p.Pro411Ser
|
|
NM_001987.4:c.1231C>T , LRG_609t1:c.1231C>T
|
NP_001978.1:p.Pro411Ser
|
|
XM_011520607.1:c.1228C>T
|
XP_011518909.1:p.Pro410Ser
|
|
XM_011520608.1:c.1204C>T
|
XP_011518910.1:p.Pro402Ser
|
|
XM_011520609.1:c.967C>T
|
XP_011518911.1:p.Pro323Ser
|
|
XM_011520610.1:c.967C>T
|
XP_011518912.1:p.Pro323Ser
|
|
XM_011520611.1:c.967C>T
|
XP_011518913.1:p.Pro323Ser
|
|
XM_011520612.1:c.610C>T
|
XP_011518914.1:p.Pro204Ser
|
|
XM_011520607.2:c.1228C>T
|
XP_011518909.1:p.Pro410Ser
|
|
XM_011520608.2:c.1204C>T
|
XP_011518910.1:p.Pro402Ser
|
|
XM_011520609.2:c.967C>T
|
XP_011518911.1:p.Pro323Ser
|
|
XM_011520611.2:c.967C>T
|
XP_011518913.1:p.Pro323Ser
|
|
XM_011520612.2:c.610C>T
|
XP_011518914.1:p.Pro204Ser
|
|
XM_017018990.1:c.1096C>T
|
XP_016874479.1:p.Pro366Ser
|
|
XM_017018991.1:c.967C>T
|
XP_016874480.1:p.Pro323Ser
|
|
NM_001987.5:c.1231C>T
MANE Select
|
NP_001978.1:p.Pro411Ser
|
|