ENST00000541682.7:c.539G>A
MANE Select
|
ENSP00000446205.2:p.Trp180Ter
|
|
ENST00000317814.8:c.524G>A
|
ENSP00000314774.4:p.Trp175Ter
|
|
ENST00000541682.6:c.539G>A
|
ENSP00000446205.2:p.Trp180Ter
|
|
NM_001165967.1:c.539G>A
|
NP_001159439.1:p.Trp180Ter
|
|
NM_032580.3:c.524G>A
|
NP_115969.2:p.Trp175Ter
|
|
XM_011524038.1:c.644G>A
|
XP_011522340.1:p.Trp215Ter
|
|
XM_011524039.1:c.635G>A
|
XP_011522341.1:p.Trp212Ter
|
|
XM_011524040.1:c.635G>A
|
XP_011522342.1:p.Trp212Ter
|
|
XM_011524041.1:c.626G>A
|
XP_011522343.1:p.Trp209Ter
|
|
XM_011524042.1:c.497G>A
|
XP_011522344.1:p.Trp166Ter
|
|
XR_934203.1:n.69+1911C>T
|
|
|
XM_017025232.1:c.644G>A
|
XP_016880721.1:p.Trp215Ter
|
|
XM_024451007.1:c.644G>A
|
XP_024306775.1:p.Trp215Ter
|
|
NM_001165967.2:c.539G>A
MANE Select
|
NP_001159439.1:p.Trp180Ter
|
|
NM_032580.4:c.524G>A
|
NP_115969.2:p.Trp175Ter
|
|