ENST00000218099.7:c.594T=
MANE Select
|
ENSP00000218099.2:p.Asp198=
|
|
ENST00000643157.1:n.1261T=
|
|
|
ENST00000218099.6:c.594T=
|
ENSP00000218099.2:p.Asp198=
|
|
ENST00000394090.2:c.480T=
|
ENSP00000377650.2:p.Asp160=
|
|
NM_000133.3:c.594T= , LRG_556t1:c.594T=
|
NP_000124.1:p.Asp198=
|
|
NM_001313913.1:c.480T=
|
NP_001300842.1:p.Asp160=
|
|
XM_005262397.3:c.465T=
|
XP_005262454.1:p.Asp155=
|
|
XM_005262397.4:c.465T=
|
XP_005262454.1:p.Asp155=
|
|
NM_000133.4:c.594T=
MANE Select
|
NP_000124.1:p.Asp198=
|
|
NM_001313913.2:c.480T=
|
NP_001300842.1:p.Asp160=
|
|