ENST00000323022.10:c.3027G>T
MANE Select
|
ENSP00000321618.6:p.Gln1009His
|
|
ENST00000323022.9:c.3027G>T
|
ENSP00000321618.5:p.Gln1009His
|
|
ENST00000376251.5:c.2865G>T
|
ENSP00000365427.1:p.Gln955His
|
|
ENST00000376265.2:c.3060G>T
|
ENSP00000365441.2:p.Gln1020His
|
|
NM_001256789.2:c.3027G>T
|
NP_001243718.1:p.Gln1009His
|
|
NM_001256790.2:c.2865G>T
|
NP_001243719.1:p.Gln955His
|
|
NM_005183.3:c.3060G>T
|
NP_005174.2:p.Gln1020His
|
|
XM_011543983.1:c.2865G>T
|
XP_011542285.1:p.Gln955His
|
|
XM_011543983.2:c.2865G>T
|
XP_011542285.1:p.Gln955His
|
|
XM_017029836.1:c.294G>T
|
XP_016885325.1:p.Gln98His
|
|
NM_001256789.3:c.3027G>T
MANE Select
|
NP_001243718.1:p.Gln1009His
|
|
NM_001256790.3:c.2865G>T
|
NP_001243719.1:p.Gln955His
|
|
NM_005183.4:c.3060G>T
|
NP_005174.2:p.Gln1020His
|
|