|
ENST00000473665.2:n.6009C>A
|
|
|
|
ENST00000482662.2:n.4416C>A
|
|
|
|
ENST00000685865.1:n.2368C>A
|
|
|
|
ENST00000687250.1:n.2068C>A
|
|
|
|
ENST00000687995.1:n.1883C>A
|
|
|
|
ENST00000688205.1:c.*1124C>A
|
ENSP00000509673.1:n.*1124C>A
|
|
|
ENST00000688788.1:n.1770C>A
|
|
|
|
ENST00000689276.1:c.1462C>A
|
ENSP00000510012.1:p.Pro488Thr
|
|
|
ENST00000689576.1:c.*150C>A
|
ENSP00000508712.1:n.*150C>A
|
|
|
ENST00000690108.1:c.*1187C>A
|
ENSP00000510617.1:n.*1187C>A
|
|
|
ENST00000690468.1:c.*83C>A
|
ENSP00000509078.1:n.*83C>A
|
|
|
ENST00000690595.1:c.856C>A
|
ENSP00000508979.1:p.Pro286Thr
|
|
|
ENST00000691348.1:c.*83C>A
|
ENSP00000509369.1:n.*83C>A
|
|
|
ENST00000691410.1:c.*1108C>A
|
ENSP00000508479.1:n.*1108C>A
|
|
|
ENST00000693287.1:c.847C>A
|
ENSP00000510264.1:p.Pro283Thr
|
|
|
ENST00000693681.1:c.844C>A
|
ENSP00000510789.1:p.Pro282Thr
|
|
|
ENST00000233838.9:c.1531C>A
MANE Select
|
ENSP00000233838.3:p.Pro511Thr
|
|
|
ENST00000233838.8:c.1531C>A
|
ENSP00000233838.3:p.Pro511Thr
|
|
|
ENST00000430215.7:c.1360C>A
|
ENSP00000408045.3:p.Pro454Thr
|
|
|
ENST00000465637.5:n.179-3886C>A
|
|
|
|
NM_000821.5:c.1531C>A
|
NP_000812.2:p.Pro511Thr
|
|
|
NM_000821.6:c.1531C>A
|
NP_000812.2:p.Pro511Thr
|
|
|
NM_001142269.2:c.1360C>A
|
NP_001135741.1:p.Pro454Thr
|
|
|
NM_001142269.3:c.1360C>A
|
NP_001135741.1:p.Pro454Thr
|
|
|
XM_005264259.3:c.1531C>A
|
XP_005264316.1:p.Pro511Thr
|
|
|
XM_011532764.1:c.709C>A
|
XP_011531066.1:p.Pro237Thr
|
|
|
XM_011532765.1:c.709C>A
|
XP_011531067.1:p.Pro237Thr
|
|
|
XR_939677.1:n.1444C>A
|
|
|
|
XM_005264259.5:c.1531C>A
|
XP_005264316.1:p.Pro511Thr
|
|
|
XM_011532764.3:c.709C>A
|
XP_011531066.1:p.Pro237Thr
|
|
|
XM_011532765.3:c.709C>A
|
XP_011531067.1:p.Pro237Thr
|
|
|
XM_017003803.2:c.1360C>A
|
XP_016859292.1:p.Pro454Thr
|
|
|
XR_001738703.2:n.1444C>A
|
|
|
|
NM_000821.7:c.1531C>A
MANE Select
|
NP_000812.2:p.Pro511Thr
|
|
|
NM_001142269.4:c.1360C>A
|
NP_001135741.1:p.Pro454Thr
|
|
