ENST00000373344.11:c.7370G>A
MANE Select
|
ENSP00000362441.4:p.Arg2457Lys
|
|
ENST00000675732.1:c.2468G>A
|
ENSP00000502598.1:p.Arg823Lys
|
|
ENST00000373344.9:c.7370G>A
|
ENSP00000362441.4:p.Arg2457Lys
|
|
ENST00000395603.7:c.7256G>A
|
ENSP00000378967.3:p.Arg2419Lys
|
|
ENST00000480283.5:c.*6998G>A
|
ENSP00000480196.1:n.*6998G>A
|
|
ENST00000623706.3:n.5690G>A
|
|
|
NM_000489.4:c.7370G>A
|
NP_000480.3:p.Arg2457Lys
|
|
NM_138270.3:c.7256G>A
|
NP_612114.2:p.Arg2419Lys
|
|
XM_005262153.3:c.7367G>A
|
XP_005262210.2:p.Arg2456Lys
|
|
XM_005262154.3:c.7283G>A
|
XP_005262211.2:p.Arg2428Lys
|
|
XM_005262155.3:c.7253G>A
|
XP_005262212.2:p.Arg2418Lys
|
|
XM_005262156.3:c.7205G>A
|
XP_005262213.2:p.Arg2402Lys
|
|
XM_005262157.3:c.7166G>A
|
XP_005262214.2:p.Arg2389Lys
|
|
XM_006724666.2:c.7253G>A
|
XP_006724729.1:p.Arg2418Lys
|
|
XM_006724667.2:c.7091G>A
|
XP_006724730.1:p.Arg2364Lys
|
|
XR_938400.1:n.8962G>A
|
|
|
NM_000489.5:c.7370G>A
|
NP_000480.3:p.Arg2457Lys
|
|
XM_005262153.5:c.7367G>A
|
XP_005262210.2:p.Arg2456Lys
|
|
XM_005262154.5:c.7283G>A
|
XP_005262211.2:p.Arg2428Lys
|
|
XM_005262155.4:c.7253G>A
|
XP_005262212.2:p.Arg2418Lys
|
|
XM_005262156.4:c.7205G>A
|
XP_005262213.2:p.Arg2402Lys
|
|
XM_005262157.5:c.7166G>A
|
XP_005262214.2:p.Arg2389Lys
|
|
XM_006724666.4:c.7253G>A
|
XP_006724729.1:p.Arg2418Lys
|
|
XM_006724667.3:c.7091G>A
|
XP_006724730.1:p.Arg2364Lys
|
|
XM_017029601.2:c.7280G>A
|
XP_016885090.1:p.Arg2427Lys
|
|
XM_017029602.1:c.7250G>A
|
XP_016885091.1:p.Arg2417Lys
|
|
XM_017029603.1:c.7202G>A
|
XP_016885092.1:p.Arg2401Lys
|
|
XM_017029604.2:c.7169G>A
|
XP_016885093.1:p.Arg2390Lys
|
|
XM_017029605.1:c.7166G>A
|
XP_016885094.1:p.Arg2389Lys
|
|
XM_017029606.2:c.7139G>A
|
XP_016885095.1:p.Arg2380Lys
|
|
XM_017029607.2:c.7136G>A
|
XP_016885096.1:p.Arg2379Lys
|
|
XM_017029608.2:c.7088G>A
|
XP_016885097.1:p.Arg2363Lys
|
|
XM_017029609.1:c.7052G>A
|
XP_016885098.1:p.Arg2351Lys
|
|
XM_017029610.1:c.7049G>A
|
XP_016885099.1:p.Arg2350Lys
|
|
XM_017029611.1:c.7004G>A
|
XP_016885100.1:p.Arg2335Lys
|
|
XR_001755700.2:n.7669G>A
|
|
|
NM_138270.4:c.7256G>A
|
NP_612114.2:p.Arg2419Lys
|
|
NM_000489.6:c.7370G>A
MANE Select
|
NP_000480.3:p.Arg2457Lys
|
|
NM_138270.5:c.7256G>A
|
NP_612114.2:p.Arg2419Lys
|
|