ENST00000292147.7:c.252C>G
(ETHE1)
MANE Select
|
ENSP00000292147.1:p.His84Gln
|
|
ENST00000292147.6:c.252C>G
(ETHE1)
|
ENSP00000292147.1:p.His84Gln
|
|
ENST00000458714.2:c.-66+86G>C
(ZNF575)
|
ENSP00000413956.2:n.-66+86G>C
|
|
ENST00000594342.5:c.226+191C>G
(ETHE1)
|
ENSP00000469652.1:n.226+191C>G
|
|
ENST00000595115.1:n.470C>G
(ETHE1)
|
|
|
ENST00000598330.1:c.226+191C>G
(ETHE1)
|
ENSP00000469219.1:n.226+191C>G
|
|
ENST00000600651.5:c.252C>G
(ETHE1)
|
ENSP00000469037.1:p.His84Gln
|
|
ENST00000602138.1:c.*256C>G
(ETHE1)
|
ENSP00000468964.1:n.*256C>G
|
|
NM_014297.3:c.252C>G
(ETHE1)
|
NP_055112.2:p.His84Gln
|
|
XM_005258687.2:c.171C>G
(ETHE1)
|
XP_005258744.1:p.His57Gln
|
|
XM_005258688.2:c.6+191C>G
(ETHE1)
|
XP_005258745.1:n.6+191C>G
|
|
XM_011526685.1:c.226+191C>G
(ETHE1)
|
XP_011524987.1:n.226+191C>G
|
|
NM_001320867.1:c.227-8C>G
(ETHE1)
|
NP_001307796.1:n.227-8C>G
|
|
NM_001320868.1:c.6+191C>G
(ETHE1)
|
NP_001307797.1:n.6+191C>G
|
|
NM_001320869.1:c.81+773C>G
(ETHE1)
|
NP_001307798.1:n.81+773C>G
|
|
NM_014297.4:c.252C>G
(ETHE1)
|
NP_055112.2:p.His84Gln
|
|
XM_005258687.4:c.171C>G
(ETHE1)
|
XP_005258744.1:p.His57Gln
|
|
NM_014297.5:c.252C>G
(ETHE1)
MANE Select
|
NP_055112.2:p.His84Gln
|
|
NM_001320867.2:c.227-8C>G
(ETHE1)
|
NP_001307796.1:n.227-8C>G
|
|
NM_001320868.2:c.6+191C>G
(ETHE1)
|
NP_001307797.1:n.6+191C>G
|
|
NM_001320869.2:c.81+773C>G
(ETHE1)
|
NP_001307798.1:n.81+773C>G
|
|