ENST00000262493.12:c.774G>C
MANE Select
|
ENSP00000262493.6:p.Lys258Asn
|
|
ENST00000562316.6:c.441G>C
|
ENSP00000457238.2:p.Lys147Asn
|
|
ENST00000564727.2:c.78G>C
|
ENSP00000454971.2:p.Lys26Asn
|
|
ENST00000568375.2:c.116-3432G>C
|
|
|
ENST00000638185.1:n.989G>C
|
|
|
ENST00000638210.1:n.1074G>C
|
|
|
ENST00000638705.1:c.774G>C
|
ENSP00000491223.1:p.Lys258Asn
|
|
ENST00000638836.1:n.684G>C
|
|
|
ENST00000639055.1:n.1495G>C
|
|
|
ENST00000639251.1:n.675G>C
|
|
|
ENST00000639268.1:c.409G>C
|
|
|
ENST00000639341.1:c.299G>C
|
|
|
ENST00000639770.1:c.812G>C
|
ENSP00000491999.1:n.812G>C
|
|
ENST00000640390.1:n.704G>C
|
|
|
ENST00000640469.1:c.138G>C
|
ENSP00000491875.1:p.Lys46Asn
|
|
ENST00000640560.1:n.550G>C
|
|
|
ENST00000640893.1:c.*172G>C
|
ENSP00000492677.1:n.*172G>C
|
|
ENST00000262493.10:c.774G>C
|
ENSP00000262493.6:p.Lys258Asn
|
|
ENST00000568375.1:n.116-3432G>C
|
|
|
NM_020988.2:c.774G>C
|
NP_066268.1:p.Lys258Asn
|
|
XM_011523003.1:c.648G>C
|
XP_011521305.1:p.Lys216Asn
|
|
XM_011523003.3:c.648G>C
|
XP_011521305.1:p.Lys216Asn
|
|
NM_020988.3:c.774G>C
MANE Select
|
NP_066268.1:p.Lys258Asn
|
|