ENST00000265104.5:c.9136G>T
MANE Select
|
ENSP00000265104.4:p.Asp3046Tyr
|
|
ENST00000681290.1:c.9091G>T
|
ENSP00000505288.1:p.Asp3031Tyr
|
|
ENST00000265104.4:c.9136G>T
|
ENSP00000265104.4:p.Asp3046Tyr
|
|
NM_001369.2:c.9136G>T
|
NP_001360.1:p.Asp3046Tyr
|
|
XM_005248262.2:c.9091G>T
|
XP_005248319.1:p.Asp3031Tyr
|
|
XM_011513990.1:c.*23G>T
|
XP_011512292.1:n.*23G>T
|
|
XR_925598.1:n.9207G>T
|
|
|
XM_005248262.3:c.9244G>T
|
XP_005248319.2:p.Asp3082Tyr
|
|
XM_017009177.1:c.9244G>T
|
XP_016864666.1:p.Asp3082Tyr
|
|
XM_017009178.1:c.8149G>T
|
XP_016864667.1:p.Asp2717Tyr
|
|
XM_017009179.2:c.8149G>T
|
XP_016864668.1:p.Asp2717Tyr
|
|
XM_017009180.1:c.9244G>T
|
XP_016864669.1:p.Asp3082Tyr
|
|
XM_017009181.1:c.9244G>T
|
XP_016864670.1:p.Asp3082Tyr
|
|
XM_017009182.1:c.9244G>T
|
XP_016864671.1:p.Asp3082Tyr
|
|
XM_017009183.1:c.9244G>T
|
XP_016864672.1:p.Asp3082Tyr
|
|
XM_017009184.1:c.*23G>T
|
XP_016864673.1:n.*23G>T
|
|
XM_017009185.1:c.4333G>T
|
XP_016864674.1:p.Asp1445Tyr
|
|
XM_017009186.1:c.3886G>T
|
XP_016864675.1:p.Asp1296Tyr
|
|
XM_017009188.1:c.3223G>T
|
XP_016864677.1:p.Asp1075Tyr
|
|
XM_024454388.1:c.8149G>T
|
XP_024310156.1:p.Asp2717Tyr
|
|
XM_024454389.1:c.7738G>T
|
XP_024310157.1:p.Asp2580Tyr
|
|
XR_001742034.1:n.9130G>T
|
|
|
XR_001742035.1:n.9125G>T
|
|
|
NM_001369.3:c.9136G>T
MANE Select
|
NP_001360.1:p.Asp3046Tyr
|
|