ENST00000426508.7:c.3529G>A
MANE Select
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ENSP00000406012.2:p.Ala1177Thr
|
|
ENST00000361339.9:c.1111G>A
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ENSP00000354895.5:p.Ala371Thr
|
|
ENST00000397417.6:c.*1967G>A
|
ENSP00000380562.2:n.*1967G>A
|
|
ENST00000426508.6:c.3529G>A
|
ENSP00000406012.2:p.Ala1177Thr
|
|
ENST00000565298.5:n.3353G>A
|
|
|
NM_014714.3:c.3529G>A
|
NP_055529.2:p.Ala1177Thr
|
|
XM_006720989.2:c.3529G>A
|
XP_006721052.1:p.Ala1177Thr
|
|
XM_006720990.2:c.3529G>A
|
XP_006721053.1:p.Ala1177Thr
|
|
XM_006720991.2:c.3529G>A
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XP_006721054.1:p.Ala1177Thr
|
|
XM_006720992.2:c.1162G>A
|
XP_006721055.1:p.Ala388Thr
|
|
XM_011522766.1:c.3283G>A
|
XP_011521068.1:p.Ala1095Thr
|
|
XM_011522767.1:c.2554G>A
|
XP_011521069.1:p.Ala852Thr
|
|
XM_006720990.3:c.3529G>A
|
XP_006721053.1:p.Ala1177Thr
|
|
XM_006720991.3:c.3529G>A
|
XP_006721054.1:p.Ala1177Thr
|
|
XM_006720992.3:c.1162G>A
|
XP_006721055.1:p.Ala388Thr
|
|
XM_011522766.3:c.3283G>A
|
XP_011521068.1:p.Ala1095Thr
|
|
XM_011522767.2:c.2554G>A
|
XP_011521069.1:p.Ala852Thr
|
|
XM_017023910.1:c.3529G>A
|
XP_016879399.1:p.Ala1177Thr
|
|
XM_017023911.1:c.1714G>A
|
XP_016879400.1:p.Ala572Thr
|
|
NM_014714.4:c.3529G>A
MANE Select
|
NP_055529.2:p.Ala1177Thr
|
|