ENST00000700075.1:c.24G>T
|
ENSP00000514784.1:p.Met8Ile
|
|
ENST00000342771.10:c.1956G>T
MANE Select
|
ENSP00000344087.4:p.Met652Ile
|
|
ENST00000439256.2:c.54G>T
|
ENSP00000407058.2:p.Met18Ile
|
|
ENST00000443672.2:c.291G>T
|
ENSP00000393548.2:p.Met97Ile
|
|
ENST00000449547.6:c.49G>T
|
|
|
ENST00000464768.2:n.624G>T
|
|
|
ENST00000644359.1:c.537G>T
|
ENSP00000494561.1:p.Met179Ile
|
|
ENST00000644506.1:c.582G>T
|
ENSP00000496672.1:p.Met194Ile
|
|
ENST00000644939.1:c.1953G>T
|
ENSP00000496726.1:p.Met651Ile
|
|
ENST00000644949.1:c.287G>T
|
|
|
ENST00000646136.1:n.267G>T
|
|
|
ENST00000647140.1:c.821G>T
|
|
|
ENST00000342771.8:c.1956G>T
|
ENSP00000344087.4:p.Met652Ile
|
|
ENST00000406775.6:c.1884G>T
|
ENSP00000385263.2:p.Met628Ile
|
|
ENST00000439256.1:c.54G>T
|
|
|
ENST00000443672.1:c.536G>T
|
|
|
ENST00000464768.1:n.622G>T
|
|
|
ENST00000465899.1:n.453G>T
|
|
|
ENST00000498384.5:n.324G>T
|
|
|
ENST00000611706.4:c.1212G>T
|
ENSP00000478134.1:p.Met404Ile
|
|
ENST00000615871.4:c.1140G>T
|
ENSP00000479325.1:p.Met380Ile
|
|
NM_001127231.2:c.1884G>T
|
NP_001120703.1:p.Met628Ile
|
|
NM_015570.3:c.1956G>T
|
NP_056385.1:p.Met652Ile
|
|
XM_005250257.1:c.603G>T
|
XP_005250314.1:p.Met201Ile
|
|
XM_011516010.1:c.1977G>T
|
XP_011514312.1:p.Met659Ile
|
|
XM_011516011.1:c.1974G>T
|
XP_011514313.1:p.Met658Ile
|
|
XM_011516012.1:c.1911G>T
|
XP_011514314.1:p.Met637Ile
|
|
XM_011516013.1:c.1905G>T
|
XP_011514315.1:p.Met635Ile
|
|
XM_011516014.1:c.1875G>T
|
XP_011514316.1:p.Met625Ile
|
|
XM_011516015.1:c.1713G>T
|
XP_011514317.1:p.Met571Ile
|
|
XM_011516016.1:c.1686G>T
|
XP_011514318.1:p.Met562Ile
|
|
XM_011516017.1:c.1503G>T
|
XP_011514319.1:p.Met501Ile
|
|
XM_011516018.1:c.1476G>T
|
XP_011514320.1:p.Met492Ile
|
|
XM_005250257.2:c.603G>T
|
XP_005250314.1:p.Met201Ile
|
|
XM_011516010.2:c.1977G>T
|
XP_011514312.1:p.Met659Ile
|
|
XM_011516011.2:c.1974G>T
|
XP_011514313.1:p.Met658Ile
|
|
XM_011516012.2:c.1911G>T
|
XP_011514314.1:p.Met637Ile
|
|
XM_011516013.2:c.1905G>T
|
XP_011514315.1:p.Met635Ile
|
|
XM_011516014.2:c.1875G>T
|
XP_011514316.1:p.Met625Ile
|
|
XM_011516017.2:c.1503G>T
|
XP_011514319.1:p.Met501Ile
|
|
XM_011516018.2:c.1476G>T
|
XP_011514320.1:p.Met492Ile
|
|
XM_017011951.2:c.1977G>T
|
XP_016867440.1:p.Met659Ile
|
|
NM_001127231.3:c.1884G>T
|
NP_001120703.1:p.Met628Ile
|
|
NM_015570.4:c.1956G>T
MANE Select
|
NP_056385.1:p.Met652Ile
|
|