|
NM_182943.3:c.1872T>G
MANE Select
|
NP_891988.1:p.Tyr624Ter
|
|
ENST00000282903.10:c.1872T>G
MANE Select
|
ENSP00000282903.5:p.Tyr624Ter
|
|
NM_000935.2:c.1809T>G
|
NP_000926.2:p.Tyr603Ter
|
|
NM_000935.3:c.1809T>G
|
NP_000926.2:p.Tyr603Ter
|
|
NM_182943.2:c.1872T>G
|
NP_891988.1:p.Tyr624Ter
|
|
ENST00000282903.9:c.1872T>G
|
ENSP00000282903.5:p.Tyr624Ter
|
|
ENST00000360060.7:c.1809T>G
|
ENSP00000353170.3:p.Tyr603Ter
|
|
ENST00000461497.5:c.852T>G
|
ENSP00000419354.1:p.Tyr284Ter
|
|
ENST00000469350.6:c.1725T>G
|
ENSP00000419963.2:p.Tyr575Ter
|
|
ENST00000480704.2:c.*1636T>G
|
ENSP00000419880.1:n.*1636T>G
|
|
ENST00000494950.5:c.1707T>G
|
ENSP00000420094.1:p.Tyr569Ter
|
|
ENST00000703517.1:n.579+31355T>G
|
|
|
ENST00000703518.1:c.1872T>G
|
ENSP00000515350.1:p.Tyr624Ter
|
|
ENST00000703519.1:n.1889T>G
|
|
|
ENST00000703520.1:c.*286T>G
|
ENSP00000515351.1:n.*286T>G
|
|
ENST00000703521.1:c.*1224T>G
|
ENSP00000515352.1:n.*1224T>G
|
|
ENST00000703522.1:c.1872T>G
|
ENSP00000515353.1:p.Tyr624Ter
|
|
ENST00000703523.1:c.1809T>G
|
ENSP00000515354.1:p.Tyr603Ter
|
|
ENST00000703524.1:n.1692T>G
|
|
|
ENST00000703525.1:n.4224T>G
|
|
|
ENST00000703526.1:n.1240T>G
|
|
|
ENST00000703527.1:c.1872T>G
|
ENSP00000515355.1:p.Tyr624Ter
|
|
ENST00000703528.1:c.1440-1306T>G
|
ENSP00000515356.1:n.1440-1306T>G
|
|
ENST00000706626.1:c.1695T>G
|
ENSP00000516472.1:p.Tyr565Ter
|
|
ENST00000706631.1:n.2317T>G
|
|
|
ENST00000706632.1:n.736T>G
|
|
|
ENST00000706633.1:n.2844T>G
|
|
|
ENST00000706634.1:n.3033T>G
|
|
|
ENST00000706635.1:c.1704T>G
|
ENSP00000516475.1:p.Tyr568Ter
|
|
ENST00000706636.1:c.*1161T>G
|
ENSP00000516476.1:n.*1161T>G
|
|
XM_005247535.3:c.1596T>G
|
XP_005247592.1:p.Tyr532Ter
|
|
XM_005247535.4:c.1596T>G
|
XP_005247592.1:p.Tyr532Ter
|
|
XM_017006625.2:c.1596T>G
|
XP_016862114.1:p.Tyr532Ter
|
|
XM_024453599.1:c.1533T>G
|
XP_024309367.1:p.Tyr511Ter
|
|
XR_001740176.2:n.2140T>G
|
|
