ENST00000308982.12:c.1304A>G
MANE Select
|
ENSP00000312618.7:p.Tyr435Cys
|
|
ENST00000511325.2:n.1382A>G
|
|
|
ENST00000679399.1:c.*1475A>G
|
ENSP00000505434.1:n.*1475A>G
|
|
ENST00000679431.1:c.*1180A>G
|
ENSP00000506440.1:n.*1180A>G
|
|
ENST00000679613.1:c.1304A>G
|
ENSP00000504971.1:p.Tyr435Cys
|
|
ENST00000679715.1:c.935A>G
|
ENSP00000506228.1:p.Tyr312Cys
|
|
ENST00000679824.1:c.*2610A>G
|
ENSP00000505516.1:n.*2610A>G
|
|
ENST00000679990.1:n.1539A>G
|
|
|
ENST00000680636.1:c.1304A>G
|
ENSP00000504886.1:p.Tyr435Cys
|
|
ENST00000680638.1:n.349A>G
|
|
|
ENST00000680744.1:c.*657A>G
|
ENSP00000505243.1:n.*657A>G
|
|
ENST00000680764.1:c.*2708A>G
|
ENSP00000505126.1:n.*2708A>G
|
|
ENST00000681319.1:n.1382A>G
|
|
|
ENST00000681367.1:c.1304A>G
|
ENSP00000505309.1:p.Tyr435Cys
|
|
ENST00000681552.1:c.1149+3705A>G
|
ENSP00000505699.1:n.1149+3705A>G
|
|
ENST00000681583.1:c.1304A>G
|
ENSP00000506340.1:p.Tyr435Cys
|
|
ENST00000681585.1:c.1304A>G
|
ENSP00000506316.1:p.Tyr435Cys
|
|
ENST00000681784.1:n.1382A>G
|
|
|
ENST00000681886.1:c.*497A>G
|
ENSP00000506500.1:n.*497A>G
|
|
ENST00000308982.11:c.1304A>G
|
ENSP00000312618.7:p.Tyr435Cys
|
|
ENST00000505192.5:c.*1000A>G
|
ENSP00000426277.1:n.*1000A>G
|
|
ENST00000505867.5:c.*1104A>G
|
ENSP00000425346.1:n.*1104A>G
|
|
ENST00000508971.1:c.593A>G
|
ENSP00000422683.1:p.Tyr198Cys
|
|
ENST00000511227.5:c.*1198A>G
|
ENSP00000425226.1:n.*1198A>G
|
|
ENST00000511325.1:n.285A>G
|
|
|
ENST00000511526.5:n.837A>G
|
|
|
NM_014049.4:c.1304A>G
|
NP_054768.2:p.Tyr435Cys
|
|
NR_033426.1:n.1682A>G
|
|
|
XM_011512742.1:c.935A>G
|
XP_011511044.1:p.Tyr312Cys
|
|
XR_427367.1:n.1380A>G
|
|
|
XM_024453484.1:c.935A>G
|
XP_024309252.1:p.Tyr312Cys
|
|
XM_024453485.1:c.935A>G
|
XP_024309253.1:p.Tyr312Cys
|
|
XR_427367.3:n.1380A>G
|
|
|
NM_014049.5:c.1304A>G
MANE Select
|
NP_054768.2:p.Tyr435Cys
|
|
NR_033426.2:n.1552A>G
|
|
|