ENST00000373344.11:c.7408C>T
MANE Select
|
ENSP00000362441.4:p.Pro2470Ser
|
|
ENST00000675732.1:c.2506C>T
|
ENSP00000502598.1:p.Pro836Ser
|
|
ENST00000373344.9:c.7408C>T
|
ENSP00000362441.4:p.Pro2470Ser
|
|
ENST00000395603.7:c.7294C>T
|
ENSP00000378967.3:p.Pro2432Ser
|
|
ENST00000480283.5:c.*7036C>T
|
ENSP00000480196.1:n.*7036C>T
|
|
ENST00000623706.3:n.5728C>T
|
|
|
NM_000489.4:c.7408C>T
|
NP_000480.3:p.Pro2470Ser
|
|
NM_138270.3:c.7294C>T
|
NP_612114.2:p.Pro2432Ser
|
|
XM_005262153.3:c.7405C>T
|
XP_005262210.2:p.Pro2469Ser
|
|
XM_005262154.3:c.7321C>T
|
XP_005262211.2:p.Pro2441Ser
|
|
XM_005262155.3:c.7291C>T
|
XP_005262212.2:p.Pro2431Ser
|
|
XM_005262156.3:c.7243C>T
|
XP_005262213.2:p.Pro2415Ser
|
|
XM_005262157.3:c.7204C>T
|
XP_005262214.2:p.Pro2402Ser
|
|
XM_006724666.2:c.7291C>T
|
XP_006724729.1:p.Pro2431Ser
|
|
XM_006724667.2:c.7129C>T
|
XP_006724730.1:p.Pro2377Ser
|
|
XR_938400.1:n.9000C>T
|
|
|
NM_000489.5:c.7408C>T
|
NP_000480.3:p.Pro2470Ser
|
|
XM_005262153.5:c.7405C>T
|
XP_005262210.2:p.Pro2469Ser
|
|
XM_005262154.5:c.7321C>T
|
XP_005262211.2:p.Pro2441Ser
|
|
XM_005262155.4:c.7291C>T
|
XP_005262212.2:p.Pro2431Ser
|
|
XM_005262156.4:c.7243C>T
|
XP_005262213.2:p.Pro2415Ser
|
|
XM_005262157.5:c.7204C>T
|
XP_005262214.2:p.Pro2402Ser
|
|
XM_006724666.4:c.7291C>T
|
XP_006724729.1:p.Pro2431Ser
|
|
XM_006724667.3:c.7129C>T
|
XP_006724730.1:p.Pro2377Ser
|
|
XM_017029601.2:c.7318C>T
|
XP_016885090.1:p.Pro2440Ser
|
|
XM_017029602.1:c.7288C>T
|
XP_016885091.1:p.Pro2430Ser
|
|
XM_017029603.1:c.7240C>T
|
XP_016885092.1:p.Pro2414Ser
|
|
XM_017029604.2:c.7207C>T
|
XP_016885093.1:p.Pro2403Ser
|
|
XM_017029605.1:c.7204C>T
|
XP_016885094.1:p.Pro2402Ser
|
|
XM_017029606.2:c.7177C>T
|
XP_016885095.1:p.Pro2393Ser
|
|
XM_017029607.2:c.7174C>T
|
XP_016885096.1:p.Pro2392Ser
|
|
XM_017029608.2:c.7126C>T
|
XP_016885097.1:p.Pro2376Ser
|
|
XM_017029609.1:c.7090C>T
|
XP_016885098.1:p.Pro2364Ser
|
|
XM_017029610.1:c.7087C>T
|
XP_016885099.1:p.Pro2363Ser
|
|
XM_017029611.1:c.7042C>T
|
XP_016885100.1:p.Pro2348Ser
|
|
XR_001755700.2:n.7707C>T
|
|
|
NM_138270.4:c.7294C>T
|
NP_612114.2:p.Pro2432Ser
|
|
NM_000489.6:c.7408C>T
MANE Select
|
NP_000480.3:p.Pro2470Ser
|
|
NM_138270.5:c.7294C>T
|
NP_612114.2:p.Pro2432Ser
|
|