ENST00000262494.13:c.649G>T
|
ENSP00000262494.7:p.Glu217Ter
|
|
ENST00000262493.12:c.649G>T
MANE Select
|
ENSP00000262493.6:p.Glu217Ter
|
|
ENST00000262494.12:c.649G>T
|
ENSP00000262494.7:p.Glu217Ter
|
|
ENST00000562316.6:c.316G>T
|
ENSP00000457238.2:p.Glu106Ter
|
|
ENST00000568375.2:c.41G>T
|
|
|
ENST00000638185.1:n.864G>T
|
|
|
ENST00000638210.1:n.949G>T
|
|
|
ENST00000638705.1:c.649G>T
|
ENSP00000491223.1:p.Glu217Ter
|
|
ENST00000638836.1:n.559G>T
|
|
|
ENST00000639055.1:n.1370G>T
|
|
|
ENST00000639251.1:n.550G>T
|
|
|
ENST00000639268.1:c.284G>T
|
|
|
ENST00000639341.1:c.174G>T
|
|
|
ENST00000639770.1:c.687G>T
|
ENSP00000491999.1:n.687G>T
|
|
ENST00000640390.1:n.579G>T
|
|
|
ENST00000640469.1:c.13G>T
|
ENSP00000491875.1:p.Glu5Ter
|
|
ENST00000640560.1:n.425G>T
|
|
|
ENST00000640893.1:c.*47G>T
|
ENSP00000492677.1:n.*47G>T
|
|
ENST00000262493.10:c.649G>T
|
ENSP00000262493.6:p.Glu217Ter
|
|
ENST00000262494.11:c.649G>T
|
ENSP00000262494.7:p.Glu217Ter
|
|
ENST00000568375.1:n.41G>T
|
|
|
NM_020988.2:c.649G>T
|
NP_066268.1:p.Glu217Ter
|
|
NM_138736.2:c.649G>T
|
NP_620073.2:p.Glu217Ter
|
|
XM_011523003.1:c.523G>T
|
XP_011521305.1:p.Glu175Ter
|
|
XM_011523003.3:c.523G>T
|
XP_011521305.1:p.Glu175Ter
|
|
NM_020988.3:c.649G>T
MANE Select
|
NP_066268.1:p.Glu217Ter
|
|
NM_138736.3:c.649G>T
|
NP_620073.2:p.Glu217Ter
|
|