ENST00000375262.4:c.704C>G
|
ENSP00000364411.2:p.Ala235Gly
|
|
ENST00000375263.8:c.854C>G
MANE Select
|
ENSP00000364412.3:p.Ala285Gly
|
|
ENST00000463517.2:n.2396C>G
|
|
|
ENST00000464104.6:n.1792C>G
|
|
|
ENST00000467499.6:c.*553C>G
|
ENSP00000498077.1:n.*553C>G
|
|
ENST00000494814.6:n.404C>G
|
|
|
ENST00000643789.1:c.3146C>G
|
|
|
ENST00000648146.1:c.992C>G
|
ENSP00000497238.1:n.992C>G
|
|
ENST00000648332.1:c.531C>G
|
ENSP00000497562.1:n.531C>G
|
|
ENST00000650005.1:c.783C>G
|
ENSP00000498121.1:n.783C>G
|
|
ENST00000375262.3:c.704C>G
|
ENSP00000364411.2:p.Ala235Gly
|
|
ENST00000375263.7:c.854C>G
|
ENSP00000364412.3:p.Ala285Gly
|
|
ENST00000464104.5:n.707C>G
|
|
|
ENST00000467499.5:n.114C>G
|
|
|
ENST00000494814.5:n.413C>G
|
|
|
NM_000197.1:c.854C>G
|
NP_000188.1:p.Ala285Gly
|
|
XM_005251970.3:c.494C>G
|
XP_005252027.1:p.Ala165Gly
|
|
XM_011518618.1:c.854C>G
|
XP_011516920.1:p.Ala285Gly
|
|
XM_011518619.1:c.854C>G
|
XP_011516921.1:p.Ala285Gly
|
|
XM_011518620.1:c.746C>G
|
XP_011516922.1:p.Ala249Gly
|
|
NM_000197.2:c.854C>G
MANE Select
|
NP_000188.1:p.Ala285Gly
|
|
XM_011518618.2:c.854C>G
|
XP_011516920.1:p.Ala285Gly
|
|
XM_011518619.2:c.854C>G
|
XP_011516921.1:p.Ala285Gly
|
|
XM_017014671.1:c.854C>G
|
XP_016870160.1:p.Ala285Gly
|
|
XM_017014672.1:c.854C>G
|
XP_016870161.1:p.Ala285Gly
|
|
XM_017014673.2:c.818C>G
|
XP_016870162.1:p.Ala273Gly
|
|
XM_017014674.1:c.746C>G
|
XP_016870163.1:p.Ala249Gly
|
|
XM_017014675.1:c.692C>G
|
XP_016870164.1:p.Ala231Gly
|
|
XM_017014677.1:c.494C>G
|
XP_016870166.1:p.Ala165Gly
|
|
XM_024447529.1:c.692C>G
|
XP_024303297.1:p.Ala231Gly
|
|
XR_002956778.1:n.3326C>G
|
|
|