ENST00000580299.2:c.2134C>T
|
ENSP00000462607.2:p.Pro712Ser
|
|
ENST00000581729.2:c.2134C>T
|
ENSP00000462720.2:p.Pro712Ser
|
|
ENST00000581967.2:n.2586C>T
|
|
|
ENST00000583254.2:n.2840C>T
|
|
|
ENST00000699849.1:c.1237C>T
|
ENSP00000514647.1:p.Pro413Ser
|
|
ENST00000699850.1:n.1397C>T
|
|
|
ENST00000699851.1:n.2156C>T
|
|
|
ENST00000699852.1:c.*810C>T
|
ENSP00000514648.1:n.*810C>T
|
|
ENST00000699853.1:c.2134C>T
|
ENSP00000514649.1:p.Pro712Ser
|
|
ENST00000699854.1:n.1927C>T
|
|
|
ENST00000699855.1:n.2586C>T
|
|
|
ENST00000699856.1:c.2134C>T
|
ENSP00000514650.1:p.Pro712Ser
|
|
ENST00000699857.1:n.2142C>T
|
|
|
ENST00000699858.1:c.*747C>T
|
ENSP00000514651.1:n.*747C>T
|
|
ENST00000699859.1:c.2005C>T
|
ENSP00000514652.1:p.Pro669Ser
|
|
ENST00000699860.1:n.240C>T
|
|
|
ENST00000699861.1:n.2156C>T
|
|
|
ENST00000699862.1:n.3094C>T
|
|
|
ENST00000449476.7:c.2029C>T
|
ENSP00000396018.2:p.Pro677Ser
|
|
ENST00000581671.2:n.2123C>T
|
|
|
ENST00000643543.1:c.*841C>T
|
ENSP00000494323.1:n.*841C>T
|
|
ENST00000651323.1:c.2134C>T
MANE Select
|
ENSP00000498499.1:p.Pro712Ser
|
|
ENST00000315684.12:c.2134C>T
|
ENSP00000313759.8:p.Pro712Ser
|
|
ENST00000449476.6:c.2029C>T
|
ENSP00000396018.2:p.Pro677Ser
|
|
ENST00000578240.1:n.362C>T
|
|
|
ENST00000578537.1:c.30C>T
|
|
|
NM_025099.5:c.2134C>T
|
NP_079375.3:p.Pro712Ser
|
|
NR_046431.1:n.2088C>T
|
|
|
XM_006721577.2:c.2005C>T
|
XP_006721640.1:p.Pro669Ser
|
|
XM_006721578.2:c.2134C>T
|
XP_006721641.1:p.Pro712Ser
|
|
XM_006721579.2:c.2134C>T
|
XP_006721642.1:p.Pro712Ser
|
|
XM_011524010.1:c.2029C>T
|
XP_011522312.1:p.Pro677Ser
|
|
XM_011524011.1:c.1237C>T
|
XP_011522313.1:p.Pro413Ser
|
|
XR_429823.2:n.2177C>T
|
|
|
XR_429824.2:n.2177C>T
|
|
|
XR_429825.1:n.2177C>T
|
|
|
NM_025099.6:c.2134C>T
MANE Select
|
NP_079375.3:p.Pro712Ser
|
|
XM_006721577.3:c.2005C>T
|
XP_006721640.1:p.Pro669Ser
|
|
XM_006721578.3:c.2134C>T
|
XP_006721641.1:p.Pro712Ser
|
|
XM_011524010.2:c.2029C>T
|
XP_011522312.1:p.Pro677Ser
|
|
XM_011524011.2:c.1237C>T
|
XP_011522313.1:p.Pro413Ser
|
|
XR_001752639.1:n.2048C>T
|
|
|
XR_001752640.1:n.2177C>T
|
|
|
XR_001752641.1:n.2177C>T
|
|
|
XR_001752642.1:n.2177C>T
|
|
|
XR_001752643.1:n.2607C>T
|
|
|
XR_002958073.1:n.2177C>T
|
|
|
XR_429823.3:n.2177C>T
|
|
|
XR_429824.3:n.2177C>T
|
|
|
NR_046431.2:n.2049C>T
|
|
|