ENST00000324041.6:c.587G=
MANE Select
|
ENSP00000326159.1:p.Gly196=
|
|
ENST00000324041.5:c.587G=
|
ENSP00000326159.1:p.Gly196=
|
|
ENST00000431178.2:c.328+195G=
|
ENSP00000399448.2:n.328+195G=
|
|
ENST00000593885.1:c.*82G=
|
ENSP00000469769.1:n.*82G=
|
|
ENST00000596876.1:n.589G=
|
|
|
ENST00000598305.5:c.*82G=
|
ENSP00000469963.1:n.*82G=
|
|
ENST00000599865.5:n.523G=
|
|
|
ENST00000602148.1:c.599G=
|
ENSP00000472091.1:n.599G=
|
|
NM_001302961.1:c.302G=
|
NP_001289890.1:p.Gly101=
|
|
NM_004917.4:c.587G=
|
NP_004908.4:p.Gly196=
|
|
NR_126566.1:n.576G=
|
|
|
XM_005259441.3:c.302G=
|
XP_005259498.2:p.Gly101=
|
|
XM_011527545.1:c.*82G=
|
XP_011525847.1:n.*82G=
|
|
XM_011527546.1:c.475+195G=
|
XP_011525848.1:n.475+195G=
|
|
XM_011527547.1:c.440G=
|
XP_011525849.1:p.Gly147=
|
|
XM_005259441.4:c.302G=
|
XP_005259498.2:p.Gly101=
|
|
XM_011527545.3:c.*82G=
|
XP_011525847.1:n.*82G=
|
|
XM_011527546.2:c.475+195G=
|
XP_011525848.1:n.475+195G=
|
|
NM_001302961.2:c.302G=
|
NP_001289890.1:p.Gly101=
|
|
NR_126566.2:n.576G=
|
|
|
NM_004917.5:c.587G=
MANE Select
|
NP_004908.4:p.Gly196=
|
|