ENST00000373344.11:c.7401G>T
MANE Select
|
ENSP00000362441.4:p.Met2467Ile
|
|
ENST00000675732.1:c.2499G>T
|
ENSP00000502598.1:p.Met833Ile
|
|
ENST00000373344.9:c.7401G>T
|
ENSP00000362441.4:p.Met2467Ile
|
|
ENST00000395603.7:c.7287G>T
|
ENSP00000378967.3:p.Met2429Ile
|
|
ENST00000480283.5:c.*7029G>T
|
ENSP00000480196.1:n.*7029G>T
|
|
ENST00000623706.3:n.5721G>T
|
|
|
NM_000489.4:c.7401G>T
|
NP_000480.3:p.Met2467Ile
|
|
NM_138270.3:c.7287G>T
|
NP_612114.2:p.Met2429Ile
|
|
XM_005262153.3:c.7398G>T
|
XP_005262210.2:p.Met2466Ile
|
|
XM_005262154.3:c.7314G>T
|
XP_005262211.2:p.Met2438Ile
|
|
XM_005262155.3:c.7284G>T
|
XP_005262212.2:p.Met2428Ile
|
|
XM_005262156.3:c.7236G>T
|
XP_005262213.2:p.Met2412Ile
|
|
XM_005262157.3:c.7197G>T
|
XP_005262214.2:p.Met2399Ile
|
|
XM_006724666.2:c.7284G>T
|
XP_006724729.1:p.Met2428Ile
|
|
XM_006724667.2:c.7122G>T
|
XP_006724730.1:p.Met2374Ile
|
|
XR_938400.1:n.8993G>T
|
|
|
NM_000489.5:c.7401G>T
|
NP_000480.3:p.Met2467Ile
|
|
XM_005262153.5:c.7398G>T
|
XP_005262210.2:p.Met2466Ile
|
|
XM_005262154.5:c.7314G>T
|
XP_005262211.2:p.Met2438Ile
|
|
XM_005262155.4:c.7284G>T
|
XP_005262212.2:p.Met2428Ile
|
|
XM_005262156.4:c.7236G>T
|
XP_005262213.2:p.Met2412Ile
|
|
XM_005262157.5:c.7197G>T
|
XP_005262214.2:p.Met2399Ile
|
|
XM_006724666.4:c.7284G>T
|
XP_006724729.1:p.Met2428Ile
|
|
XM_006724667.3:c.7122G>T
|
XP_006724730.1:p.Met2374Ile
|
|
XM_017029601.2:c.7311G>T
|
XP_016885090.1:p.Met2437Ile
|
|
XM_017029602.1:c.7281G>T
|
XP_016885091.1:p.Met2427Ile
|
|
XM_017029603.1:c.7233G>T
|
XP_016885092.1:p.Met2411Ile
|
|
XM_017029604.2:c.7200G>T
|
XP_016885093.1:p.Met2400Ile
|
|
XM_017029605.1:c.7197G>T
|
XP_016885094.1:p.Met2399Ile
|
|
XM_017029606.2:c.7170G>T
|
XP_016885095.1:p.Met2390Ile
|
|
XM_017029607.2:c.7167G>T
|
XP_016885096.1:p.Met2389Ile
|
|
XM_017029608.2:c.7119G>T
|
XP_016885097.1:p.Met2373Ile
|
|
XM_017029609.1:c.7083G>T
|
XP_016885098.1:p.Met2361Ile
|
|
XM_017029610.1:c.7080G>T
|
XP_016885099.1:p.Met2360Ile
|
|
XM_017029611.1:c.7035G>T
|
XP_016885100.1:p.Met2345Ile
|
|
XR_001755700.2:n.7700G>T
|
|
|
NM_138270.4:c.7287G>T
|
NP_612114.2:p.Met2429Ile
|
|
NM_000489.6:c.7401G>T
MANE Select
|
NP_000480.3:p.Met2467Ile
|
|
NM_138270.5:c.7287G>T
|
NP_612114.2:p.Met2429Ile
|
|