ENST00000355773.6:c.1325T>A
MANE Select
|
ENSP00000348019.5:p.Val442Asp
|
|
ENST00000355773.5:c.1325T>A
|
ENSP00000348019.5:p.Val442Asp
|
|
NM_012434.4:c.1325T>A
|
NP_036566.1:p.Val442Asp
|
|
XM_005248710.2:c.1274T>A
|
XP_005248767.1:p.Val425Asp
|
|
XM_005248711.1:c.1127T>A
|
XP_005248768.1:p.Val376Asp
|
|
XM_011535750.1:c.1177T>A
|
XP_011534052.1:p.Ser393Thr
|
|
NM_012434.5:c.1325T>A
MANE Select
|
NP_036566.1:p.Val442Asp
|
|
NM_001382629.1:c.1094T>A
|
NP_001369558.1:p.Val365Asp
|
|
NM_001382630.1:c.1260-5162T>A
|
NP_001369559.1:n.1260-5162T>A
|
|
NM_001382631.1:c.1346T>A
|
NP_001369560.1:p.Val449Asp
|
|
NM_001382632.1:c.1238T>A
|
NP_001369561.1:p.Val413Asp
|
|
NM_001382633.1:c.1325T>A
|
NP_001369562.1:p.Val442Asp
|
|
NM_001382634.1:c.1166T>A
|
NP_001369563.1:p.Val389Asp
|
|
NM_001382635.1:c.1322T>A
|
NP_001369564.1:p.Val441Asp
|
|
NM_001382636.1:c.1007T>A
|
NP_001369565.1:p.Val336Asp
|
|