ENST00000373344.11:c.7390G>C
MANE Select
|
ENSP00000362441.4:p.Ala2464Pro
|
|
ENST00000675732.1:c.2488G>C
|
ENSP00000502598.1:p.Ala830Pro
|
|
ENST00000373344.9:c.7390G>C
|
ENSP00000362441.4:p.Ala2464Pro
|
|
ENST00000395603.7:c.7276G>C
|
ENSP00000378967.3:p.Ala2426Pro
|
|
ENST00000480283.5:c.*7018G>C
|
ENSP00000480196.1:n.*7018G>C
|
|
ENST00000623706.3:n.5710G>C
|
|
|
NM_000489.4:c.7390G>C
|
NP_000480.3:p.Ala2464Pro
|
|
NM_138270.3:c.7276G>C
|
NP_612114.2:p.Ala2426Pro
|
|
XM_005262153.3:c.7387G>C
|
XP_005262210.2:p.Ala2463Pro
|
|
XM_005262154.3:c.7303G>C
|
XP_005262211.2:p.Ala2435Pro
|
|
XM_005262155.3:c.7273G>C
|
XP_005262212.2:p.Ala2425Pro
|
|
XM_005262156.3:c.7225G>C
|
XP_005262213.2:p.Ala2409Pro
|
|
XM_005262157.3:c.7186G>C
|
XP_005262214.2:p.Ala2396Pro
|
|
XM_006724666.2:c.7273G>C
|
XP_006724729.1:p.Ala2425Pro
|
|
XM_006724667.2:c.7111G>C
|
XP_006724730.1:p.Ala2371Pro
|
|
XR_938400.1:n.8982G>C
|
|
|
NM_000489.5:c.7390G>C
|
NP_000480.3:p.Ala2464Pro
|
|
XM_005262153.5:c.7387G>C
|
XP_005262210.2:p.Ala2463Pro
|
|
XM_005262154.5:c.7303G>C
|
XP_005262211.2:p.Ala2435Pro
|
|
XM_005262155.4:c.7273G>C
|
XP_005262212.2:p.Ala2425Pro
|
|
XM_005262156.4:c.7225G>C
|
XP_005262213.2:p.Ala2409Pro
|
|
XM_005262157.5:c.7186G>C
|
XP_005262214.2:p.Ala2396Pro
|
|
XM_006724666.4:c.7273G>C
|
XP_006724729.1:p.Ala2425Pro
|
|
XM_006724667.3:c.7111G>C
|
XP_006724730.1:p.Ala2371Pro
|
|
XM_017029601.2:c.7300G>C
|
XP_016885090.1:p.Ala2434Pro
|
|
XM_017029602.1:c.7270G>C
|
XP_016885091.1:p.Ala2424Pro
|
|
XM_017029603.1:c.7222G>C
|
XP_016885092.1:p.Ala2408Pro
|
|
XM_017029604.2:c.7189G>C
|
XP_016885093.1:p.Ala2397Pro
|
|
XM_017029605.1:c.7186G>C
|
XP_016885094.1:p.Ala2396Pro
|
|
XM_017029606.2:c.7159G>C
|
XP_016885095.1:p.Ala2387Pro
|
|
XM_017029607.2:c.7156G>C
|
XP_016885096.1:p.Ala2386Pro
|
|
XM_017029608.2:c.7108G>C
|
XP_016885097.1:p.Ala2370Pro
|
|
XM_017029609.1:c.7072G>C
|
XP_016885098.1:p.Ala2358Pro
|
|
XM_017029610.1:c.7069G>C
|
XP_016885099.1:p.Ala2357Pro
|
|
XM_017029611.1:c.7024G>C
|
XP_016885100.1:p.Ala2342Pro
|
|
XR_001755700.2:n.7689G>C
|
|
|
NM_138270.4:c.7276G>C
|
NP_612114.2:p.Ala2426Pro
|
|
NM_000489.6:c.7390G>C
MANE Select
|
NP_000480.3:p.Ala2464Pro
|
|
NM_138270.5:c.7276G>C
|
NP_612114.2:p.Ala2426Pro
|
|