ENST00000262493.12:c.727C>T
MANE Select
|
ENSP00000262493.6:p.Arg243Cys
|
|
ENST00000562316.6:c.394C>T
|
ENSP00000457238.2:p.Arg132Cys
|
|
ENST00000564727.2:c.31C>T
|
ENSP00000454971.2:p.Arg11Cys
|
|
ENST00000568375.2:c.116-3479C>T
|
|
|
ENST00000638185.1:n.942C>T
|
|
|
ENST00000638210.1:n.1027C>T
|
|
|
ENST00000638705.1:c.727C>T
|
ENSP00000491223.1:p.Arg243Cys
|
|
ENST00000638836.1:n.637C>T
|
|
|
ENST00000639055.1:n.1448C>T
|
|
|
ENST00000639251.1:n.628C>T
|
|
|
ENST00000639268.1:c.362C>T
|
|
|
ENST00000639341.1:c.252C>T
|
|
|
ENST00000639770.1:c.765C>T
|
ENSP00000491999.1:n.765C>T
|
|
ENST00000640390.1:n.657C>T
|
|
|
ENST00000640469.1:c.91C>T
|
ENSP00000491875.1:p.Arg31Cys
|
|
ENST00000640560.1:n.503C>T
|
|
|
ENST00000640893.1:c.*125C>T
|
ENSP00000492677.1:n.*125C>T
|
|
ENST00000262493.10:c.727C>T
|
ENSP00000262493.6:p.Arg243Cys
|
|
ENST00000568375.1:n.116-3479C>T
|
|
|
NM_020988.2:c.727C>T
|
NP_066268.1:p.Arg243Cys
|
|
XM_011523003.1:c.601C>T
|
XP_011521305.1:p.Arg201Cys
|
|
XM_011523003.3:c.601C>T
|
XP_011521305.1:p.Arg201Cys
|
|
NM_020988.3:c.727C>T
MANE Select
|
NP_066268.1:p.Arg243Cys
|
|