|
ENST00000581113.7:c.10G>T
|
ENSP00000492721.2:p.Ala4Ser
|
|
|
ENST00000696138.1:c.4204G>T
|
ENSP00000512431.1:p.Ala1402Ser
|
|
|
ENST00000696140.1:n.328G>T
|
|
|
|
ENST00000696141.1:c.213G>T
|
|
|
|
ENST00000687863.1:n.867G>T
|
|
|
|
ENST00000691014.1:c.4252G>T
|
ENSP00000510595.1:p.Ala1418Ser
|
|
|
ENST00000691649.1:n.194G>T
|
|
|
|
ENST00000358273.9:c.4222G>T
MANE Select
|
ENSP00000351015.4:p.Ala1408Ser
|
|
|
ENST00000356175.7:c.4159G>T
|
ENSP00000348498.3:p.Ala1387Ser
|
|
|
ENST00000358273.8:c.4222G>T
|
ENSP00000351015.4:p.Ala1408Ser
|
|
|
ENST00000456735.6:c.3157G>T
|
ENSP00000389907.2:p.Ala1053Ser
|
|
|
ENST00000466819.5:c.738G>T
|
|
|
|
ENST00000479614.1:c.675G>T
|
|
|
|
ENST00000493220.5:n.2695G>T
|
|
|
|
ENST00000579081.5:c.4261G>T
|
ENSP00000462408.1:p.Ala1421Ser
|
|
|
NM_000267.3:c.4159G>T , LRG_214t1:c.4159G>T
|
NP_000258.1:p.Ala1387Ser
|
|
|
NM_001042492.2:c.4222G>T , LRG_214t2:c.4222G>T
|
NP_001035957.1:p.Ala1408Ser
|
|
|
XM_005257983.1:c.4222G>T
|
XP_005258040.1:p.Ala1408Ser
|
|
|
XM_005257984.1:c.4159G>T
|
XP_005258041.1:p.Ala1387Ser
|
|
|
XM_006721922.1:c.4252G>T
|
XP_006721985.1:p.Ala1418Ser
|
|
|
XM_006721923.2:c.4213G>T
|
XP_006721986.1:p.Ala1405Ser
|
|
|
XM_006721924.1:c.4252G>T
|
XP_006721987.1:p.Ala1418Ser
|
|
|
XM_006721925.1:c.4189G>T
|
XP_006721988.1:p.Ala1397Ser
|
|
|
XM_006721926.2:c.4252G>T
|
XP_006721989.1:p.Ala1418Ser
|
|
|
XM_006721927.1:c.4252G>T
|
XP_006721990.1:p.Ala1418Ser
|
|
|
XM_006721928.2:c.4252G>T
|
XP_006721991.1:p.Ala1418Ser
|
|
|
XM_011524852.1:c.4249G>T
|
XP_011523154.1:p.Ala1417Ser
|
|
|
XM_011524853.1:c.4213G>T
|
XP_011523155.1:p.Ala1405Ser
|
|
|
XM_011524854.1:c.4213G>T
|
XP_011523156.1:p.Ala1405Ser
|
|
|
XM_011524855.1:c.4213G>T
|
XP_011523157.1:p.Ala1405Ser
|
|
|
XM_011524856.1:c.4213G>T
|
XP_011523158.1:p.Ala1405Ser
|
|
|
XM_011524857.1:c.4252G>T
|
XP_011523159.1:p.Ala1418Ser
|
|
|
NM_001042492.3:c.4222G>T
MANE Select
|
NP_001035957.1:p.Ala1408Ser
|
|
