ENST00000460843.6:c.1803G>T
MANE Select
|
ENSP00000417980.1:p.Met601Ile
|
|
ENST00000636027.1:c.1689G>T
|
ENSP00000489961.1:p.Met563Ile
|
|
ENST00000637161.1:c.1710G>T
|
ENSP00000490328.1:p.Met570Ile
|
|
ENST00000637261.1:c.1843G>T
|
ENSP00000490815.1:n.1843G>T
|
|
ENST00000638071.1:c.1430G>T
|
|
|
ENST00000640639.1:c.972G>T
|
ENSP00000491823.1:p.Met324Ile
|
|
ENST00000371394.6:c.*1538G>T
|
ENSP00000485945.1:n.*1538G>T
|
|
ENST00000460843.5:c.1803G>T
|
ENSP00000417980.1:p.Met601Ile
|
|
ENST00000462484.5:c.1803G>T
|
ENSP00000417328.1:p.Met601Ile
|
|
ENST00000462942.3:c.660G>T
|
ENSP00000436107.1:p.Met220Ile
|
|
ENST00000465566.2:c.351G>T
|
ENSP00000486261.1:p.Met117Ile
|
|
ENST00000626603.1:n.1820C>A
|
|
|
NM_001145527.1:c.1803G>T
|
NP_001138999.1:p.Met601Ile
|
|
NM_024757.4:c.1803G>T
|
NP_079033.4:p.Met601Ile
|
|
XM_005266105.3:c.1794G>T
|
XP_005266162.1:p.Met598Ile
|
|
XM_005266110.1:c.1710G>T
|
XP_005266167.1:p.Met570Ile
|
|
XM_006717288.2:c.1785G>T
|
XP_006717351.1:p.Met595Ile
|
|
XM_011519021.1:c.1812G>T
|
XP_011517323.1:p.Met604Ile
|
|
XM_011519022.1:c.1809G>T
|
XP_011517324.1:p.Met603Ile
|
|
XM_011519023.1:c.1791G>T
|
XP_011517325.1:p.Met597Ile
|
|
XM_011519024.1:c.1734G>T
|
XP_011517326.1:p.Met578Ile
|
|
XM_011519025.1:c.1710G>T
|
XP_011517327.1:p.Met570Ile
|
|
XM_011519026.1:c.1668G>T
|
XP_011517328.1:p.Met556Ile
|
|
XM_011519027.1:c.1812G>T
|
XP_011517329.1:p.Met604Ile
|
|
XM_011519028.1:c.1812G>T
|
XP_011517330.1:p.Met604Ile
|
|
XM_011519029.1:c.234G>T
|
XP_011517331.1:p.Met78Ile
|
|
XM_011519033.1:c.1647G>T
|
XP_011517335.1:p.Met549Ile
|
|
NM_001354259.1:c.1710G>T
|
NP_001341188.1:p.Met570Ile
|
|
NM_001354263.1:c.1782G>T
|
NP_001341192.1:p.Met594Ile
|
|
XM_005266105.5:c.1794G>T
|
XP_005266162.1:p.Met598Ile
|
|
XM_011519021.3:c.1812G>T
|
XP_011517323.1:p.Met604Ile
|
|
XM_011519022.3:c.1809G>T
|
XP_011517324.1:p.Met603Ile
|
|
XM_011519023.3:c.1791G>T
|
XP_011517325.1:p.Met597Ile
|
|
XM_011519029.3:c.234G>T
|
XP_011517331.1:p.Met78Ile
|
|
XM_017015134.1:c.1788G>T
|
XP_016870623.1:p.Met596Ile
|
|
XM_017015136.2:c.1704G>T
|
XP_016870625.1:p.Met568Ile
|
|
XM_017015137.1:c.1689G>T
|
XP_016870626.1:p.Met563Ile
|
|
XM_017015138.1:c.1689G>T
|
XP_016870627.1:p.Met563Ile
|
|
XM_024447674.1:c.1632G>T
|
XP_024303442.1:p.Met544Ile
|
|
XM_024447675.1:c.1566G>T
|
XP_024303443.1:p.Met522Ile
|
|
XM_024447676.1:c.927G>T
|
XP_024303444.1:p.Met309Ile
|
|
XM_024447677.1:c.927G>T
|
XP_024303445.1:p.Met309Ile
|
|
XM_024447678.1:c.1710G>T
|
XP_024303446.1:p.Met570Ile
|
|
XM_024447679.1:c.1710G>T
|
XP_024303447.1:p.Met570Ile
|
|
XM_024447680.1:c.1545G>T
|
XP_024303448.1:p.Met515Ile
|
|
NM_024757.5:c.1803G>T
MANE Select
|
NP_079033.4:p.Met601Ile
|
|
NM_001145527.2:c.1803G>T
|
NP_001138999.1:p.Met601Ile
|
|
NM_001354259.2:c.1710G>T
|
NP_001341188.1:p.Met570Ile
|
|
NM_001354263.2:c.1782G>T
|
NP_001341192.1:p.Met594Ile
|
|