ENST00000328194.8:c.3669C>G
MANE Select
|
ENSP00000328524.3:p.Cys1223Trp
|
|
ENST00000525784.6:n.1531C>G
|
|
|
ENST00000530780.2:c.*3495C>G
|
ENSP00000433925.1:n.*3495C>G
|
|
ENST00000531747.2:n.3340C>G
|
|
|
ENST00000679446.1:n.3590C>G
|
|
|
ENST00000679458.1:n.5070C>G
|
|
|
ENST00000679460.1:n.4731C>G
|
|
|
ENST00000679568.1:c.3669C>G
|
ENSP00000505860.1:p.Cys1223Trp
|
|
ENST00000679745.1:n.4174C>G
|
|
|
ENST00000679773.1:n.2830C>G
|
|
|
ENST00000679926.1:n.4971C>G
|
|
|
ENST00000679999.1:c.*726C>G
|
ENSP00000505198.1:n.*726C>G
|
|
ENST00000680252.1:c.3336C>G
|
|
|
ENST00000680294.1:c.3462C>G
|
ENSP00000506113.1:p.Cys1154Trp
|
|
ENST00000680358.1:n.2968C>G
|
|
|
ENST00000680470.1:c.*1450C>G
|
ENSP00000505975.1:n.*1450C>G
|
|
ENST00000680554.1:c.*202C>G
|
ENSP00000505621.1:n.*202C>G
|
|
ENST00000680576.1:n.5145C>G
|
|
|
ENST00000680599.1:n.3710C>G
|
|
|
ENST00000680742.1:c.*179+23C>G
|
ENSP00000505206.1:n.*179+23C>G
|
|
ENST00000680791.1:n.2553C>G
|
|
|
ENST00000680885.1:n.5371C>G
|
|
|
ENST00000681158.1:c.3253C>G
|
|
|
ENST00000681203.1:c.3597C>G
|
ENSP00000506456.1:p.Cys1199Trp
|
|
ENST00000681371.1:n.3541C>G
|
|
|
ENST00000681425.1:n.4147C>G
|
|
|
ENST00000681639.1:n.1948C>G
|
|
|
ENST00000328194.7:c.3669C>G
|
ENSP00000328524.3:p.Cys1223Trp
|
|
ENST00000525784.5:c.605C>G
|
|
|
ENST00000527700.5:n.3231C>G
|
|
|
ENST00000528725.5:c.365C>G
|
|
|
ENST00000529977.5:n.1570C>G
|
|
|
ENST00000530044.5:c.3646+23C>G
|
ENSP00000435866.1:n.3646+23C>G
|
|
ENST00000531747.1:c.905C>G
|
|
|
ENST00000533737.5:c.332C>G
|
|
|
NM_001243254.1:c.3646+23C>G
|
NP_001230183.1:n.3646+23C>G
|
|
NM_015213.3:c.3669C>G
|
NP_056028.2:p.Cys1223Trp
|
|
XM_005252832.1:c.3669C>G
|
XP_005252889.1:p.Cys1223Trp
|
|
XM_011519952.1:c.3646+23C>G
|
XP_011518254.1:n.3646+23C>G
|
|
XM_011519953.1:c.1767C>G
|
XP_011518255.1:p.Cys589Trp
|
|
XR_242782.2:n.3851C>G
|
|
|
XR_930851.1:n.3828+23C>G
|
|
|
NM_001348749.1:c.3597C>G
|
NP_001335678.1:p.Cys1199Trp
|
|
NM_001348750.1:c.3381C>G
|
NP_001335679.1:p.Cys1127Trp
|
|
NR_145966.2:n.3843C>G
|
|
|
NM_015213.4:c.3669C>G
MANE Select
|
NP_056028.2:p.Cys1223Trp
|
|
NM_001243254.2:c.3646+23C>G
|
NP_001230183.1:n.3646+23C>G
|
|
NM_001348749.2:c.3597C>G
|
NP_001335678.1:p.Cys1199Trp
|
|
NM_001348750.2:c.3381C>G
|
NP_001335679.1:p.Cys1127Trp
|
|