ENST00000262493.12:c.854C>A
MANE Select
|
ENSP00000262493.6:p.Thr285Asn
|
|
ENST00000562316.6:c.521C>A
|
ENSP00000457238.2:p.Thr174Asn
|
|
ENST00000564727.2:c.158C>A
|
ENSP00000454971.2:p.Thr53Asn
|
|
ENST00000568375.2:c.116-3352C>A
|
|
|
ENST00000638185.1:n.1069C>A
|
|
|
ENST00000638210.1:n.1154C>A
|
|
|
ENST00000638705.1:c.854C>A
|
ENSP00000491223.1:p.Thr285Asn
|
|
ENST00000638836.1:n.764C>A
|
|
|
ENST00000639055.1:n.1575C>A
|
|
|
ENST00000639251.1:n.755C>A
|
|
|
ENST00000639268.1:c.489C>A
|
|
|
ENST00000639341.1:c.379C>A
|
|
|
ENST00000639770.1:c.892C>A
|
ENSP00000491999.1:n.892C>A
|
|
ENST00000640390.1:n.784C>A
|
|
|
ENST00000640469.1:c.218C>A
|
ENSP00000491875.1:p.Thr73Asn
|
|
ENST00000640560.1:n.630C>A
|
|
|
ENST00000640893.1:c.*252C>A
|
ENSP00000492677.1:n.*252C>A
|
|
ENST00000262493.10:c.854C>A
|
ENSP00000262493.6:p.Thr285Asn
|
|
ENST00000564727.1:c.74C>A
|
ENSP00000454971.1:p.Thr25Asn
|
|
ENST00000568375.1:n.116-3352C>A
|
|
|
NM_020988.2:c.854C>A
|
NP_066268.1:p.Thr285Asn
|
|
XM_011523003.1:c.728C>A
|
XP_011521305.1:p.Thr243Asn
|
|
XM_011523003.3:c.728C>A
|
XP_011521305.1:p.Thr243Asn
|
|
NM_020988.3:c.854C>A
MANE Select
|
NP_066268.1:p.Thr285Asn
|
|