|
ENST00000696138.1:c.1251C>G
|
ENSP00000512431.1:p.Ile417Met
|
|
|
ENST00000686189.1:c.666C>G
|
ENSP00000509682.1:p.Ile222Met
|
|
|
ENST00000688507.1:n.957C>G
|
|
|
|
ENST00000691014.1:c.1251C>G
|
ENSP00000510595.1:p.Ile417Met
|
|
|
ENST00000692326.1:n.1534C>G
|
|
|
|
ENST00000358273.9:c.1251C>G
MANE Select
|
ENSP00000351015.4:p.Ile417Met
|
|
|
ENST00000356175.7:c.1251C>G
|
ENSP00000348498.3:p.Ile417Met
|
|
|
ENST00000358273.8:c.1251C>G
|
ENSP00000351015.4:p.Ile417Met
|
|
|
ENST00000431387.8:c.1251C>G
|
ENSP00000412921.4:p.Ile417Met
|
|
|
ENST00000456735.6:c.249C>G
|
ENSP00000389907.2:p.Ile83Met
|
|
|
ENST00000487476.5:n.1634C>G
|
|
|
|
ENST00000495910.6:c.1026C>G
|
|
|
|
ENST00000579081.5:c.1353C>G
|
ENSP00000462408.1:p.Ile451Met
|
|
|
NM_000267.3:c.1251C>G , LRG_214t1:c.1251C>G
|
NP_000258.1:p.Ile417Met
|
|
|
NM_001042492.2:c.1251C>G , LRG_214t2:c.1251C>G
|
NP_001035957.1:p.Ile417Met
|
|
|
NM_001128147.2:c.1251C>G
|
NP_001121619.1:p.Ile417Met
|
|
|
XM_005257983.1:c.1251C>G
|
XP_005258040.1:p.Ile417Met
|
|
|
XM_005257984.1:c.1251C>G
|
XP_005258041.1:p.Ile417Met
|
|
|
XM_006721922.1:c.1251C>G
|
XP_006721985.1:p.Ile417Met
|
|
|
XM_006721923.2:c.1212C>G
|
XP_006721986.1:p.Ile404Met
|
|
|
XM_006721924.1:c.1251C>G
|
XP_006721987.1:p.Ile417Met
|
|
|
XM_006721925.1:c.1251C>G
|
XP_006721988.1:p.Ile417Met
|
|
|
XM_006721926.2:c.1251C>G
|
XP_006721989.1:p.Ile417Met
|
|
|
XM_006721927.1:c.1251C>G
|
XP_006721990.1:p.Ile417Met
|
|
|
XM_006721928.2:c.1251C>G
|
XP_006721991.1:p.Ile417Met
|
|
|
XM_011524852.1:c.1251C>G
|
XP_011523154.1:p.Ile417Met
|
|
|
XM_011524853.1:c.1212C>G
|
XP_011523155.1:p.Ile404Met
|
|
|
XM_011524854.1:c.1212C>G
|
XP_011523156.1:p.Ile404Met
|
|
|
XM_011524855.1:c.1212C>G
|
XP_011523157.1:p.Ile404Met
|
|
|
XM_011524856.1:c.1212C>G
|
XP_011523158.1:p.Ile404Met
|
|
|
XM_011524857.1:c.1251C>G
|
XP_011523159.1:p.Ile417Met
|
|
|
NM_001042492.3:c.1251C>G
MANE Select
|
NP_001035957.1:p.Ile417Met
|
|
|
NM_001128147.3:c.1251C>G
|
NP_001121619.1:p.Ile417Met
|
|
