|
NM_032119.4:c.12935G>A
MANE Select
|
NP_115495.3:p.Gly4312Asp
|
|
ENST00000405460.9:c.12935G>A
MANE Select
|
ENSP00000384582.2:p.Gly4312Asp
|
|
NM_032119.3:c.12935G>A
|
NP_115495.3:p.Gly4312Asp
|
|
NR_003149.1:n.12948G>A
|
|
|
NR_003149.2:n.12951G>A
|
|
|
ENST00000405460.6:c.12935G>A
|
ENSP00000384582.2:p.Gly4312Asp
|
|
ENST00000425867.3:c.1889G>A
|
ENSP00000392618.3:p.Gly630Asp
|
|
ENST00000639431.1:c.265+102741G>A
|
ENSP00000491057.1:n.265+102741G>A
|
|
ENST00000640464.1:n.3354G>A
|
|
|
XM_011543675.1:c.12932G>A
|
XP_011541977.1:p.Gly4311Asp
|
|
XM_011543676.1:c.12854G>A
|
XP_011541978.1:p.Gly4285Asp
|
|
XM_011543677.1:c.10238G>A
|
XP_011541979.1:p.Gly3413Asp
|
|
XM_011543678.1:c.12935G>A
|
XP_011541980.1:p.Gly4312Asp
|
|
XM_017009963.2:c.12956G>A
|
XP_016865452.1:p.Gly4319Asp
|
|
XM_017009964.2:c.12953G>A
|
XP_016865453.1:p.Gly4318Asp
|
|
XM_017009965.1:c.12953G>A
|
XP_016865454.1:p.Gly4318Asp
|
|
XM_017009966.2:c.12875G>A
|
XP_016865455.1:p.Gly4292Asp
|
|
XM_017009967.1:c.12860G>A
|
XP_016865456.1:p.Gly4287Asp
|
|
XM_017009968.2:c.12956G>A
|
XP_016865457.1:p.Gly4319Asp
|
|
XM_017009969.2:c.12956G>A
|
XP_016865458.1:p.Gly4319Asp
|
|
XM_017009970.2:c.12956G>A
|
XP_016865459.1:p.Gly4319Asp
|
|
XM_017009971.2:c.12956G>A
|
XP_016865460.1:p.Gly4319Asp
|
|
XM_017009972.1:c.6074G>A
|
XP_016865461.1:p.Gly2025Asp
|
|
XM_017009973.1:c.6053G>A
|
XP_016865462.1:p.Gly2018Asp
|