ENST00000391944.8:c.2336G>T
|
ENSP00000375808.4:p.Arg779Met
|
|
ENST00000682414.1:c.2190+146G>T
|
ENSP00000507019.1:n.2190+146G>T
|
|
ENST00000682508.1:n.2219+146G>T
|
|
|
ENST00000684218.1:c.*1448+146G>T
|
ENSP00000507804.1:n.*1448+146G>T
|
|
ENST00000684264.1:n.1746+146G>T
|
|
|
ENST00000684407.1:c.2067+146G>T
|
ENSP00000507775.1:n.2067+146G>T
|
|
ENST00000684458.1:c.*676+146G>T
|
ENSP00000508260.1:n.*676+146G>T
|
|
ENST00000684468.1:n.1902+146G>T
|
|
|
ENST00000391945.10:c.2190+146G>T
MANE Select
|
ENSP00000375809.4:n.2190+146G>T
|
|
ENST00000646507.1:n.2287+146G>T
|
|
|
ENST00000391942.6:n.1361+146G>T
|
|
|
ENST00000391944.7:c.1956+146G>T
|
ENSP00000375808.3:n.1956+146G>T
|
|
ENST00000391945.8:c.2190+146G>T
|
ENSP00000375809.3:n.2190+146G>T
|
|
ENST00000588652.5:n.2278+146G>T
|
|
|
NM_000400.3:c.2190+146G>T , LRG_461t1:c.2190+146G>T
|
NP_000391.1:n.2190+146G>T
|
|
XM_011526611.1:c.2112+146G>T
|
XP_011524913.1:n.2112+146G>T
|
|
XM_011526611.2:c.2112+146G>T
|
XP_011524913.1:n.2112+146G>T
|
|
XM_017026467.1:c.2067+146G>T
|
XP_016881956.1:n.2067+146G>T
|
|
XR_001753633.2:n.2237+146G>T
|
|
|
XR_001753634.2:n.2173+146G>T
|
|
|
NM_000400.4:c.2190+146G>T
MANE Select
|
NP_000391.1:n.2190+146G>T
|
|