ENST00000696946.1:n.1423A>T
|
|
|
ENST00000302347.10:c.2288A>T
|
ENSP00000303242.6:p.Glu763Val
|
|
ENST00000652462.1:c.2216A>T
MANE Select
|
ENSP00000498780.1:p.Glu739Val
|
|
ENST00000302347.9:c.2216A>T
|
ENSP00000303242.5:p.Glu739Val
|
|
ENST00000355153.8:c.2216A>T
|
ENSP00000347279.4:p.Glu739Val
|
|
ENST00000397850.6:c.2216A>T
|
ENSP00000380948.2:p.Glu739Val
|
|
ENST00000397852.5:c.2216A>T
|
ENSP00000380950.1:p.Glu739Val
|
|
ENST00000397854.7:c.2045A>T
|
ENSP00000380952.3:p.Glu682Val
|
|
ENST00000397857.5:c.2216A>T
|
ENSP00000380955.1:p.Glu739Val
|
|
ENST00000475170.5:n.1616A>T
|
|
|
ENST00000479202.5:n.575A>T
|
|
|
ENST00000498666.5:n.4272A>T
|
|
|
ENST00000523323.5:c.*2043A>T
|
ENSP00000427732.1:n.*2043A>T
|
|
ENST00000610622.4:c.*907A>T
|
ENSP00000480700.1:n.*907A>T
|
|
NM_000211.4:c.2216A>T
|
NP_000202.3:p.Glu739Val
|
|
NM_001127491.2:c.2216A>T
|
NP_001120963.2:p.Glu739Val
|
|
NM_001303238.1:c.2009A>T
|
NP_001290167.1:p.Glu670Val
|
|
XM_006724001.1:c.2009A>T
|
XP_006724064.1:p.Glu670Val
|
|
XM_006724001.2:c.2009A>T
|
XP_006724064.1:p.Glu670Val
|
|
NM_000211.5:c.2216A>T
MANE Select
|
NP_000202.3:p.Glu739Val
|
|
NM_001127491.3:c.2216A>T
|
NP_001120963.2:p.Glu739Val
|
|
NM_001303238.2:c.2009A>T
|
NP_001290167.1:p.Glu670Val
|
|