ENST00000391944.8:c.2139T=
|
ENSP00000375808.4:p.Gly713=
|
|
ENST00000682414.1:c.2139T=
|
ENSP00000507019.1:p.Gly713=
|
|
ENST00000682508.1:n.2168T=
|
|
|
ENST00000684218.1:c.*1397T=
|
ENSP00000507804.1:n.*1397T=
|
|
ENST00000684264.1:n.1695T=
|
|
|
ENST00000684407.1:c.2016T=
|
ENSP00000507775.1:p.Gly672=
|
|
ENST00000684458.1:c.*625T=
|
ENSP00000508260.1:n.*625T=
|
|
ENST00000684468.1:n.1851T=
|
|
|
ENST00000391945.10:c.2139T=
MANE Select
|
ENSP00000375809.4:p.Gly713=
|
|
ENST00000646507.1:n.2236T=
|
|
|
ENST00000391941.6:c.2067T=
|
ENSP00000375805.2:p.Gly689=
|
|
ENST00000391942.6:n.1310T=
|
|
|
ENST00000391944.7:c.1905T=
|
ENSP00000375808.3:p.Gly635=
|
|
ENST00000391945.8:c.2139T=
|
ENSP00000375809.3:p.Gly713=
|
|
ENST00000588652.5:n.2227T=
|
|
|
NM_000400.3:c.2139T= , LRG_461t1:c.2139T=
|
NP_000391.1:p.Gly713=
|
|
XM_011526611.1:c.2061T=
|
XP_011524913.1:p.Gly687=
|
|
XM_011526611.2:c.2061T=
|
XP_011524913.1:p.Gly687=
|
|
XM_017026467.1:c.2016T=
|
XP_016881956.1:p.Gly672=
|
|
XR_001753633.2:n.2186T=
|
|
|
XR_001753634.2:n.2122T=
|
|
|
NM_000400.4:c.2139T=
MANE Select
|
NP_000391.1:p.Gly713=
|
|