ENST00000456935.7:c.1407G>A
MANE Select
|
ENSP00000395473.2:p.Trp469Ter
|
|
ENST00000221363.8:c.1404G>A
|
ENSP00000221363.4:p.Trp468Ter
|
|
ENST00000456935.6:c.1407G>A
|
ENSP00000395473.2:p.Trp469Ter
|
|
ENST00000465830.1:n.571G>A
|
|
|
ENST00000466794.5:n.1306G>A
|
|
|
ENST00000495617.1:n.583G>A
|
|
|
ENST00000593686.1:c.17G>A
|
|
|
NM_000528.3:c.1407G>A
|
NP_000519.2:p.Trp469Ter
|
|
NM_001173498.1:c.1404G>A
|
NP_001166969.1:p.Trp468Ter
|
|
XM_005259913.1:c.1410G>A
|
XP_005259970.1:p.Trp470Ter
|
|
XM_011528017.1:c.306G>A
|
XP_011526319.1:p.Trp102Ter
|
|
XM_005259913.2:c.1410G>A
|
XP_005259970.1:p.Trp470Ter
|
|
XM_024451518.1:c.306G>A
|
XP_024307286.1:p.Trp102Ter
|
|
NM_000528.4:c.1407G>A
MANE Select
|
NP_000519.2:p.Trp469Ter
|
|
NM_001173498.2:c.1404G>A
|
NP_001166969.1:p.Trp468Ter
|
|