|
ENST00000473665.2:n.5170T>A
|
|
|
|
ENST00000482662.2:n.3577T>A
|
|
|
|
ENST00000685865.1:n.1529T>A
|
|
|
|
ENST00000687250.1:n.1229T>A
|
|
|
|
ENST00000687995.1:n.1478T>A
|
|
|
|
ENST00000688205.1:c.*719T>A
|
ENSP00000509673.1:n.*719T>A
|
|
|
ENST00000688788.1:n.1365T>A
|
|
|
|
ENST00000689276.1:c.1057T>A
|
ENSP00000510012.1:p.Phe353Ile
|
|
|
ENST00000689576.1:c.1126T>A
|
ENSP00000508712.1:p.Phe376Ile
|
|
|
ENST00000690108.1:c.*782T>A
|
ENSP00000510617.1:n.*782T>A
|
|
|
ENST00000690468.1:c.847T>A
|
ENSP00000509078.1:p.Phe283Ile
|
|
|
ENST00000690595.1:c.451T>A
|
ENSP00000508979.1:p.Phe151Ile
|
|
|
ENST00000691348.1:c.955T>A
|
ENSP00000509369.1:p.Phe319Ile
|
|
|
ENST00000691410.1:c.*703T>A
|
ENSP00000508479.1:n.*703T>A
|
|
|
ENST00000693287.1:c.442T>A
|
ENSP00000510264.1:p.Phe148Ile
|
|
|
ENST00000693681.1:c.439T>A
|
ENSP00000510789.1:p.Phe147Ile
|
|
|
ENST00000233838.9:c.1126T>A
MANE Select
|
ENSP00000233838.3:p.Phe376Ile
|
|
|
ENST00000233838.8:c.1126T>A
|
ENSP00000233838.3:p.Phe376Ile
|
|
|
ENST00000430215.7:c.955T>A
|
ENSP00000408045.3:p.Phe319Ile
|
|
|
ENST00000465637.5:n.179-5257T>A
|
|
|
|
ENST00000473665.1:n.619T>A
|
|
|
|
ENST00000482662.1:n.543T>A
|
|
|
|
NM_000821.5:c.1126T>A
|
NP_000812.2:p.Phe376Ile
|
|
|
NM_000821.6:c.1126T>A
|
NP_000812.2:p.Phe376Ile
|
|
|
NM_001142269.2:c.955T>A
|
NP_001135741.1:p.Phe319Ile
|
|
|
NM_001142269.3:c.955T>A
|
NP_001135741.1:p.Phe319Ile
|
|
|
XM_005264259.3:c.1126T>A
|
XP_005264316.1:p.Phe376Ile
|
|
|
XM_011532764.1:c.304T>A
|
XP_011531066.1:p.Phe102Ile
|
|
|
XM_011532765.1:c.304T>A
|
XP_011531067.1:p.Phe102Ile
|
|
|
XR_939677.1:n.1191T>A
|
|
|
|
XM_005264259.5:c.1126T>A
|
XP_005264316.1:p.Phe376Ile
|
|
|
XM_011532764.3:c.304T>A
|
XP_011531066.1:p.Phe102Ile
|
|
|
XM_011532765.3:c.304T>A
|
XP_011531067.1:p.Phe102Ile
|
|
|
XM_017003803.2:c.955T>A
|
XP_016859292.1:p.Phe319Ile
|
|
|
XR_001738703.2:n.1191T>A
|
|
|
|
NM_000821.7:c.1126T>A
MANE Select
|
NP_000812.2:p.Phe376Ile
|
|
|
NM_001142269.4:c.955T>A
|
NP_001135741.1:p.Phe319Ile
|
|
