ENST00000262493.12:c.834G>C
MANE Select
|
ENSP00000262493.6:p.Lys278Asn
|
|
ENST00000562316.6:c.501G>C
|
ENSP00000457238.2:p.Lys167Asn
|
|
ENST00000564727.2:c.138G>C
|
ENSP00000454971.2:p.Lys46Asn
|
|
ENST00000568375.2:c.116-3372G>C
|
|
|
ENST00000638185.1:n.1049G>C
|
|
|
ENST00000638210.1:n.1134G>C
|
|
|
ENST00000638705.1:c.834G>C
|
ENSP00000491223.1:p.Lys278Asn
|
|
ENST00000638836.1:n.744G>C
|
|
|
ENST00000639055.1:n.1555G>C
|
|
|
ENST00000639251.1:n.735G>C
|
|
|
ENST00000639268.1:c.469G>C
|
|
|
ENST00000639341.1:c.359G>C
|
|
|
ENST00000639770.1:c.872G>C
|
ENSP00000491999.1:n.872G>C
|
|
ENST00000640390.1:n.764G>C
|
|
|
ENST00000640469.1:c.198G>C
|
ENSP00000491875.1:p.Lys66Asn
|
|
ENST00000640560.1:n.610G>C
|
|
|
ENST00000640893.1:c.*232G>C
|
ENSP00000492677.1:n.*232G>C
|
|
ENST00000262493.10:c.834G>C
|
ENSP00000262493.6:p.Lys278Asn
|
|
ENST00000564727.1:c.54G>C
|
ENSP00000454971.1:p.Lys18Asn
|
|
ENST00000568375.1:n.116-3372G>C
|
|
|
NM_020988.2:c.834G>C
|
NP_066268.1:p.Lys278Asn
|
|
XM_011523003.1:c.708G>C
|
XP_011521305.1:p.Lys236Asn
|
|
XM_011523003.3:c.708G>C
|
XP_011521305.1:p.Lys236Asn
|
|
NM_020988.3:c.834G>C
MANE Select
|
NP_066268.1:p.Lys278Asn
|
|