ENST00000373344.11:c.7368G>C
MANE Select
|
ENSP00000362441.4:p.Met2456Ile
|
|
ENST00000675732.1:c.2466G>C
|
ENSP00000502598.1:p.Met822Ile
|
|
ENST00000373344.9:c.7368G>C
|
ENSP00000362441.4:p.Met2456Ile
|
|
ENST00000395603.7:c.7254G>C
|
ENSP00000378967.3:p.Met2418Ile
|
|
ENST00000480283.5:c.*6996G>C
|
ENSP00000480196.1:n.*6996G>C
|
|
ENST00000623706.3:n.5688G>C
|
|
|
NM_000489.4:c.7368G>C
|
NP_000480.3:p.Met2456Ile
|
|
NM_138270.3:c.7254G>C
|
NP_612114.2:p.Met2418Ile
|
|
XM_005262153.3:c.7365G>C
|
XP_005262210.2:p.Met2455Ile
|
|
XM_005262154.3:c.7281G>C
|
XP_005262211.2:p.Met2427Ile
|
|
XM_005262155.3:c.7251G>C
|
XP_005262212.2:p.Met2417Ile
|
|
XM_005262156.3:c.7203G>C
|
XP_005262213.2:p.Met2401Ile
|
|
XM_005262157.3:c.7164G>C
|
XP_005262214.2:p.Met2388Ile
|
|
XM_006724666.2:c.7251G>C
|
XP_006724729.1:p.Met2417Ile
|
|
XM_006724667.2:c.7089G>C
|
XP_006724730.1:p.Met2363Ile
|
|
XR_938400.1:n.8960G>C
|
|
|
NM_000489.5:c.7368G>C
|
NP_000480.3:p.Met2456Ile
|
|
XM_005262153.5:c.7365G>C
|
XP_005262210.2:p.Met2455Ile
|
|
XM_005262154.5:c.7281G>C
|
XP_005262211.2:p.Met2427Ile
|
|
XM_005262155.4:c.7251G>C
|
XP_005262212.2:p.Met2417Ile
|
|
XM_005262156.4:c.7203G>C
|
XP_005262213.2:p.Met2401Ile
|
|
XM_005262157.5:c.7164G>C
|
XP_005262214.2:p.Met2388Ile
|
|
XM_006724666.4:c.7251G>C
|
XP_006724729.1:p.Met2417Ile
|
|
XM_006724667.3:c.7089G>C
|
XP_006724730.1:p.Met2363Ile
|
|
XM_017029601.2:c.7278G>C
|
XP_016885090.1:p.Met2426Ile
|
|
XM_017029602.1:c.7248G>C
|
XP_016885091.1:p.Met2416Ile
|
|
XM_017029603.1:c.7200G>C
|
XP_016885092.1:p.Met2400Ile
|
|
XM_017029604.2:c.7167G>C
|
XP_016885093.1:p.Met2389Ile
|
|
XM_017029605.1:c.7164G>C
|
XP_016885094.1:p.Met2388Ile
|
|
XM_017029606.2:c.7137G>C
|
XP_016885095.1:p.Met2379Ile
|
|
XM_017029607.2:c.7134G>C
|
XP_016885096.1:p.Met2378Ile
|
|
XM_017029608.2:c.7086G>C
|
XP_016885097.1:p.Met2362Ile
|
|
XM_017029609.1:c.7050G>C
|
XP_016885098.1:p.Met2350Ile
|
|
XM_017029610.1:c.7047G>C
|
XP_016885099.1:p.Met2349Ile
|
|
XM_017029611.1:c.7002G>C
|
XP_016885100.1:p.Met2334Ile
|
|
XR_001755700.2:n.7667G>C
|
|
|
NM_138270.4:c.7254G>C
|
NP_612114.2:p.Met2418Ile
|
|
NM_000489.6:c.7368G>C
MANE Select
|
NP_000480.3:p.Met2456Ile
|
|
NM_138270.5:c.7254G>C
|
NP_612114.2:p.Met2418Ile
|
|