ENST00000373344.11:c.7476G>A
MANE Select
|
ENSP00000362441.4:p.Met2492Ile
|
|
ENST00000675732.1:c.2574G>A
|
ENSP00000502598.1:p.Met858Ile
|
|
ENST00000373344.9:c.7476G>A
|
ENSP00000362441.4:p.Met2492Ile
|
|
ENST00000395603.7:c.7362G>A
|
ENSP00000378967.3:p.Met2454Ile
|
|
ENST00000480283.5:c.*7104G>A
|
ENSP00000480196.1:n.*7104G>A
|
|
ENST00000623706.3:n.5796G>A
|
|
|
NM_000489.4:c.7476G>A
|
NP_000480.3:p.Met2492Ile
|
|
NM_138270.3:c.7362G>A
|
NP_612114.2:p.Met2454Ile
|
|
XM_005262153.3:c.7473G>A
|
XP_005262210.2:p.Met2491Ile
|
|
XM_005262154.3:c.7389G>A
|
XP_005262211.2:p.Met2463Ile
|
|
XM_005262155.3:c.7359G>A
|
XP_005262212.2:p.Met2453Ile
|
|
XM_005262156.3:c.7311G>A
|
XP_005262213.2:p.Met2437Ile
|
|
XM_005262157.3:c.7272G>A
|
XP_005262214.2:p.Met2424Ile
|
|
XM_006724666.2:c.7359G>A
|
XP_006724729.1:p.Met2453Ile
|
|
XM_006724667.2:c.7197G>A
|
XP_006724730.1:p.Met2399Ile
|
|
XR_938400.1:n.9068G>A
|
|
|
NM_000489.5:c.7476G>A
|
NP_000480.3:p.Met2492Ile
|
|
XM_005262153.5:c.7473G>A
|
XP_005262210.2:p.Met2491Ile
|
|
XM_005262154.5:c.7389G>A
|
XP_005262211.2:p.Met2463Ile
|
|
XM_005262155.4:c.7359G>A
|
XP_005262212.2:p.Met2453Ile
|
|
XM_005262156.4:c.7311G>A
|
XP_005262213.2:p.Met2437Ile
|
|
XM_005262157.5:c.7272G>A
|
XP_005262214.2:p.Met2424Ile
|
|
XM_006724666.4:c.7359G>A
|
XP_006724729.1:p.Met2453Ile
|
|
XM_006724667.3:c.7197G>A
|
XP_006724730.1:p.Met2399Ile
|
|
XM_017029601.2:c.7386G>A
|
XP_016885090.1:p.Met2462Ile
|
|
XM_017029602.1:c.7356G>A
|
XP_016885091.1:p.Met2452Ile
|
|
XM_017029603.1:c.7308G>A
|
XP_016885092.1:p.Met2436Ile
|
|
XM_017029604.2:c.7275G>A
|
XP_016885093.1:p.Met2425Ile
|
|
XM_017029605.1:c.7272G>A
|
XP_016885094.1:p.Met2424Ile
|
|
XM_017029606.2:c.7245G>A
|
XP_016885095.1:p.Met2415Ile
|
|
XM_017029607.2:c.7242G>A
|
XP_016885096.1:p.Met2414Ile
|
|
XM_017029608.2:c.7194G>A
|
XP_016885097.1:p.Met2398Ile
|
|
XM_017029609.1:c.7158G>A
|
XP_016885098.1:p.Met2386Ile
|
|
XM_017029610.1:c.7155G>A
|
XP_016885099.1:p.Met2385Ile
|
|
XM_017029611.1:c.7110G>A
|
XP_016885100.1:p.Met2370Ile
|
|
XR_001755700.2:n.7775G>A
|
|
|
NM_138270.4:c.7362G>A
|
NP_612114.2:p.Met2454Ile
|
|
NM_000489.6:c.7476G>A
MANE Select
|
NP_000480.3:p.Met2492Ile
|
|
NM_138270.5:c.7362G>A
|
NP_612114.2:p.Met2454Ile
|
|