|
ENST00000696138.1:c.3722C>T
|
ENSP00000512431.1:p.Ala1241Val
|
|
|
ENST00000696139.1:c.1022C>T
|
ENSP00000512432.1:p.Ala341Val
|
|
|
ENST00000691014.1:c.3707C>T
|
ENSP00000510595.1:p.Ala1236Val
|
|
|
ENST00000693210.1:n.403C>T
|
|
|
|
ENST00000358273.9:c.3677C>T
MANE Select
|
ENSP00000351015.4:p.Ala1226Val
|
|
|
ENST00000356175.7:c.3677C>T
|
ENSP00000348498.3:p.Ala1226Val
|
|
|
ENST00000358273.8:c.3677C>T
|
ENSP00000351015.4:p.Ala1226Val
|
|
|
ENST00000456735.6:c.2675C>T
|
ENSP00000389907.2:p.Ala892Val
|
|
|
ENST00000466819.5:c.153C>T
|
|
|
|
ENST00000479614.1:c.153C>T
|
|
|
|
ENST00000493220.5:n.2213C>T
|
|
|
|
ENST00000495910.6:c.3452C>T
|
|
|
|
ENST00000579081.5:c.3779C>T
|
ENSP00000462408.1:p.Ala1260Val
|
|
|
NM_000267.3:c.3677C>T , LRG_214t1:c.3677C>T
|
NP_000258.1:p.Ala1226Val
|
|
|
NM_001042492.2:c.3677C>T , LRG_214t2:c.3677C>T
|
NP_001035957.1:p.Ala1226Val
|
|
|
XM_005257983.1:c.3677C>T
|
XP_005258040.1:p.Ala1226Val
|
|
|
XM_005257984.1:c.3677C>T
|
XP_005258041.1:p.Ala1226Val
|
|
|
XM_006721922.1:c.3707C>T
|
XP_006721985.1:p.Ala1236Val
|
|
|
XM_006721923.2:c.3668C>T
|
XP_006721986.1:p.Ala1223Val
|
|
|
XM_006721924.1:c.3707C>T
|
XP_006721987.1:p.Ala1236Val
|
|
|
XM_006721925.1:c.3707C>T
|
XP_006721988.1:p.Ala1236Val
|
|
|
XM_006721926.2:c.3707C>T
|
XP_006721989.1:p.Ala1236Val
|
|
|
XM_006721927.1:c.3707C>T
|
XP_006721990.1:p.Ala1236Val
|
|
|
XM_006721928.2:c.3707C>T
|
XP_006721991.1:p.Ala1236Val
|
|
|
XM_011524852.1:c.3704C>T
|
XP_011523154.1:p.Ala1235Val
|
|
|
XM_011524853.1:c.3668C>T
|
XP_011523155.1:p.Ala1223Val
|
|
|
XM_011524854.1:c.3668C>T
|
XP_011523156.1:p.Ala1223Val
|
|
|
XM_011524855.1:c.3668C>T
|
XP_011523157.1:p.Ala1223Val
|
|
|
XM_011524856.1:c.3668C>T
|
XP_011523158.1:p.Ala1223Val
|
|
|
XM_011524857.1:c.3707C>T
|
XP_011523159.1:p.Ala1236Val
|
|
|
NM_001042492.3:c.3677C>T
MANE Select
|
NP_001035957.1:p.Ala1226Val
|
|
