|
ENST00000696138.1:c.6692C>T
|
ENSP00000512431.1:p.Ala2231Val
|
|
|
ENST00000684826.1:c.1274C>T
|
ENSP00000509994.1:p.Ala425Val
|
|
|
ENST00000684998.1:n.1968C>T
|
|
|
|
ENST00000687027.1:c.866C>T
|
ENSP00000508715.1:p.Ala289Val
|
|
|
ENST00000687863.1:n.3355C>T
|
|
|
|
ENST00000691014.1:c.6740C>T
|
ENSP00000510595.1:p.Ala2247Val
|
|
|
ENST00000693617.1:c.1274C>T
|
ENSP00000510031.1:p.Ala425Val
|
|
|
ENST00000358273.9:c.6710C>T
MANE Select
|
ENSP00000351015.4:p.Ala2237Val
|
|
|
ENST00000356175.7:c.6647C>T
|
ENSP00000348498.3:p.Ala2216Val
|
|
|
ENST00000358273.8:c.6710C>T
|
ENSP00000351015.4:p.Ala2237Val
|
|
|
ENST00000456735.6:c.5645C>T
|
ENSP00000389907.2:p.Ala1882Val
|
|
|
ENST00000471572.6:c.93C>T
|
|
|
|
ENST00000579081.5:c.6846C>T
|
ENSP00000462408.1:n.6846C>T
|
|
|
ENST00000581790.5:c.64+150C>T
|
|
|
|
ENST00000584328.1:n.124C>T
|
|
|
|
NM_000267.3:c.6647C>T , LRG_214t1:c.6647C>T
|
NP_000258.1:p.Ala2216Val
|
|
|
NM_001042492.2:c.6710C>T , LRG_214t2:c.6710C>T
|
NP_001035957.1:p.Ala2237Val
|
|
|
XM_005257983.1:c.6710C>T
|
XP_005258040.1:p.Ala2237Val
|
|
|
XM_005257984.1:c.6647C>T
|
XP_005258041.1:p.Ala2216Val
|
|
|
XM_006721922.1:c.6740C>T
|
XP_006721985.1:p.Ala2247Val
|
|
|
XM_006721923.2:c.6701C>T
|
XP_006721986.1:p.Ala2234Val
|
|
|
XM_006721924.1:c.6740C>T
|
XP_006721987.1:p.Ala2247Val
|
|
|
XM_006721925.1:c.6677C>T
|
XP_006721988.1:p.Ala2226Val
|
|
|
XM_006721926.2:c.6740C>T
|
XP_006721989.1:p.Ala2247Val
|
|
|
XM_006721927.1:c.6740C>T
|
XP_006721990.1:p.Ala2247Val
|
|
|
XM_011524852.1:c.6737C>T
|
XP_011523154.1:p.Ala2246Val
|
|
|
XM_011524853.1:c.6701C>T
|
XP_011523155.1:p.Ala2234Val
|
|
|
XM_011524854.1:c.6701C>T
|
XP_011523156.1:p.Ala2234Val
|
|
|
XM_011524855.1:c.6701C>T
|
XP_011523157.1:p.Ala2234Val
|
|
|
XM_011524856.1:c.6701C>T
|
XP_011523158.1:p.Ala2234Val
|
|
|
XM_011524857.1:c.6740C>T
|
XP_011523159.1:p.Ala2247Val
|
|
|
NM_001042492.3:c.6710C>T
MANE Select
|
NP_001035957.1:p.Ala2237Val
|
|
