ENST00000264867.7:c.1216G>C
MANE Select
|
ENSP00000264867.2:p.Asp406His
|
|
ENST00000264867.6:c.1216G>C
|
ENSP00000264867.2:p.Asp406His
|
|
ENST00000506055.5:c.*431G>C
|
ENSP00000423075.1:n.*431G>C
|
|
ENST00000509702.5:n.1256G>C
|
|
|
ENST00000613098.4:c.835G>C
|
ENSP00000481498.1:p.Asp279His
|
|
NM_013261.3:c.1216G>C
|
NP_037393.1:p.Asp406His
|
|
XM_005248130.2:c.1231G>C
|
XP_005248187.1:p.Asp411His
|
|
XM_005248131.3:c.1228G>C
|
XP_005248188.1:p.Asp410His
|
|
XM_005248132.1:c.1207G>C
|
XP_005248189.1:p.Asp403His
|
|
XM_005248134.3:c.1231G>C
|
XP_005248191.1:p.Asp411His
|
|
XM_011513764.1:c.1216G>C
|
XP_011512066.1:p.Asp406His
|
|
XM_011513765.1:c.1180G>C
|
XP_011512067.1:p.Asp394His
|
|
XM_011513766.1:c.1111G>C
|
XP_011512068.1:p.Asp371His
|
|
XM_011513767.1:c.1111G>C
|
XP_011512069.1:p.Asp371His
|
|
XM_011513768.1:c.1111G>C
|
XP_011512070.1:p.Asp371His
|
|
XM_011513769.1:c.1231G>C
|
XP_011512071.1:p.Asp411His
|
|
XM_011513770.1:c.835G>C
|
XP_011512072.1:p.Asp279His
|
|
XM_011513771.1:c.835G>C
|
XP_011512073.1:p.Asp279His
|
|
NM_001330751.1:c.1231G>C
|
NP_001317680.1:p.Asp411His
|
|
NM_001330752.1:c.1180G>C
|
NP_001317681.1:p.Asp394His
|
|
NM_001330753.1:c.835G>C
|
NP_001317682.1:p.Asp279His
|
|
NM_001354825.1:c.1231G>C
|
NP_001341754.1:p.Asp411His
|
|
NM_001354826.1:c.835G>C
|
NP_001341755.1:p.Asp279His
|
|
NM_001354827.1:c.1231G>C
|
NP_001341756.1:p.Asp411His
|
|
NM_013261.4:c.1216G>C
|
NP_037393.1:p.Asp406His
|
|
NR_148981.1:n.1743G>C
|
|
|
NR_148982.1:n.1816G>C
|
|
|
NR_148983.1:n.1969G>C
|
|
|
NR_148984.1:n.1367G>C
|
|
|
NR_148985.1:n.1881G>C
|
|
|
NR_148986.1:n.1886G>C
|
|
|
NR_148987.1:n.1968G>C
|
|
|
XM_005248131.5:c.1228G>C
|
XP_005248188.1:p.Asp410His
|
|
XM_005248134.4:c.1231G>C
|
XP_005248191.1:p.Asp411His
|
|
XM_011513769.2:c.1231G>C
|
XP_011512071.1:p.Asp411His
|
|
XM_024453878.1:c.1231G>C
|
XP_024309646.1:p.Asp411His
|
|
NM_013261.5:c.1216G>C
MANE Select
|
NP_037393.1:p.Asp406His
|
|
NM_001330751.2:c.1231G>C
|
NP_001317680.1:p.Asp411His
|
|
NM_001330752.2:c.1180G>C
|
NP_001317681.1:p.Asp394His
|
|
NM_001354825.2:c.1231G>C
|
NP_001341754.1:p.Asp411His
|
|
NM_001354826.2:c.835G>C
|
NP_001341755.1:p.Asp279His
|
|
NM_001354827.2:c.1231G>C
|
NP_001341756.1:p.Asp411His
|
|
NR_148981.2:n.1819G>C
|
|
|
NR_148982.2:n.1892G>C
|
|
|
NR_148983.2:n.2045G>C
|
|
|
NR_148984.2:n.1337G>C
|
|
|
NR_148985.2:n.1957G>C
|
|
|
NR_148986.2:n.1962G>C
|
|
|
NR_148987.2:n.2044G>C
|
|
|
NM_001330753.2:c.835G>C
|
NP_001317682.1:p.Asp279His
|
|