ENST00000316594.6:c.536G>T
(HNRNPH2)
MANE Select
|
ENSP00000361927.2:p.Arg179Met
|
|
ENST00000316594.5:c.536G>T
(HNRNPH2)
|
ENSP00000361927.2:p.Arg179Met
|
|
NM_001032393.2:c.536G>T
(HNRNPH2)
|
NP_001027565.1:p.Arg179Met
|
|
NM_001199973.1:c.*532G>T
(RPL36A-HNRNPH2)
|
NP_001186902.1:n.*532G>T
|
|
NM_001199974.1:c.*532G>T
(RPL36A-HNRNPH2)
|
NP_001186903.1:n.*532G>T
|
|
NM_019597.4:c.536G>T
(HNRNPH2)
|
NP_062543.1:p.Arg179Met
|
|
NM_001199973.2:c.*532G>T
(RPL36A-HNRNPH2)
|
NP_001186902.2:n.*532G>T
|
|
NM_001199974.2:c.*532G>T
(RPL36A-HNRNPH2)
|
NP_001186903.2:n.*532G>T
|
|
NM_019597.5:c.536G>T
(HNRNPH2)
MANE Select
|
NP_062543.1:p.Arg179Met
|
|
NM_001032393.3:c.536G>T
(HNRNPH2)
|
NP_001027565.1:p.Arg179Met
|
|