ENST00000378888.10:c.1849C>T
MANE Select
|
ENSP00000368166.5:p.Arg617Ter
|
|
ENST00000378888.9:c.1849C>T
|
ENSP00000368166.5:p.Arg617Ter
|
|
ENST00000378891.9:c.1774C>T
|
ENSP00000368169.5:p.Arg592Ter
|
|
ENST00000610709.2:c.1096C>T
|
ENSP00000480077.1:p.Arg366Ter
|
|
NM_004421.2:c.1774C>T
|
NP_004412.2:p.Arg592Ter
|
|
XM_005244731.2:c.1849C>T
|
XP_005244788.1:p.Arg617Ter
|
|
NM_001330311.1:c.1849C>T
|
NP_001317240.1:p.Arg617Ter
|
|
XM_005244732.4:c.*162C>T
|
XP_005244789.1:n.*162C>T
|
|
XM_005244733.4:c.*162C>T
|
XP_005244790.1:n.*162C>T
|
|
NM_001330311.2:c.1849C>T
MANE Select
|
NP_001317240.1:p.Arg617Ter
|
|
NM_004421.3:c.1774C>T
|
NP_004412.2:p.Arg592Ter
|
|