ENST00000288840.10:c.981G>C
MANE Select
|
ENSP00000288840.5:p.Lys327Asn
|
|
ENST00000288840.9:c.981G>C
|
ENSP00000288840.5:p.Lys327Asn
|
|
ENST00000557916.5:c.1113G>C
|
ENSP00000452955.1:n.1113G>C
|
|
ENST00000559931.5:c.285G>C
|
ENSP00000453446.1:n.285G>C
|
|
NM_005585.4:c.981G>C
|
NP_005576.3:p.Lys327Asn
|
|
NR_027654.1:n.2036G>C
|
|
|
XM_011521561.1:c.198G>C
|
XP_011519863.1:p.Lys66Asn
|
|
XR_931825.1:n.2380G>C
|
|
|
XM_011521561.2:c.198G>C
|
XP_011519863.1:p.Lys66Asn
|
|
NM_005585.5:c.981G>C
MANE Select
|
NP_005576.3:p.Lys327Asn
|
|
NR_027654.2:n.2136G>C
|
|
|