ENST00000324041.6:c.533G>T
MANE Select
|
ENSP00000326159.1:p.Cys178Phe
|
|
ENST00000324041.5:c.533G>T
|
ENSP00000326159.1:p.Cys178Phe
|
|
ENST00000431178.2:c.328+141G>T
|
ENSP00000399448.2:n.328+141G>T
|
|
ENST00000593885.1:c.*28G>T
|
ENSP00000469769.1:n.*28G>T
|
|
ENST00000596876.1:n.535G>T
|
|
|
ENST00000598305.5:c.*28G>T
|
ENSP00000469963.1:n.*28G>T
|
|
ENST00000599865.5:n.469G>T
|
|
|
ENST00000602148.1:c.545G>T
|
ENSP00000472091.1:n.545G>T
|
|
NM_001302961.1:c.248G>T
|
NP_001289890.1:p.Cys83Phe
|
|
NM_004917.4:c.533G>T
|
NP_004908.4:p.Cys178Phe
|
|
NR_126566.1:n.522G>T
|
|
|
XM_005259441.3:c.248G>T
|
XP_005259498.2:p.Cys83Phe
|
|
XM_011527545.1:c.*28G>T
|
XP_011525847.1:n.*28G>T
|
|
XM_011527546.1:c.475+141G>T
|
XP_011525848.1:n.475+141G>T
|
|
XM_011527547.1:c.386G>T
|
XP_011525849.1:p.Cys129Phe
|
|
XM_005259441.4:c.248G>T
|
XP_005259498.2:p.Cys83Phe
|
|
XM_011527545.3:c.*28G>T
|
XP_011525847.1:n.*28G>T
|
|
XM_011527546.2:c.475+141G>T
|
XP_011525848.1:n.475+141G>T
|
|
NM_001302961.2:c.248G>T
|
NP_001289890.1:p.Cys83Phe
|
|
NR_126566.2:n.522G>T
|
|
|
NM_004917.5:c.533G>T
MANE Select
|
NP_004908.4:p.Cys178Phe
|
|