ENST00000318471.5:c.903G>C
MANE Select
|
ENSP00000315680.3:p.Gln301His
|
|
ENST00000541292.6:c.*168G>C
|
ENSP00000441004.1:n.*168G>C
|
|
ENST00000678002.1:c.591G>C
|
|
|
ENST00000678557.1:c.789G>C
|
ENSP00000502962.1:p.Gln263His
|
|
ENST00000679286.1:c.783G>C
|
ENSP00000503168.1:p.Gln261His
|
|
ENST00000318471.4:c.903G>C
|
ENSP00000315680.3:p.Gln301His
|
|
NM_000288.3:c.903G>C
|
NP_000279.1:p.Gln301His
|
|
XM_005267019.3:c.789G>C
|
XP_005267076.1:p.Gln263His
|
|
XM_006715502.1:c.609G>C
|
XP_006715565.1:p.Gln203His
|
|
XM_005267019.4:c.789G>C
|
XP_005267076.1:p.Gln263His
|
|
XM_006715502.2:c.609G>C
|
XP_006715565.1:p.Gln203His
|
|
XM_017010934.2:c.*26G>C
|
XP_016866423.1:n.*26G>C
|
|
NM_000288.4:c.903G>C
MANE Select
|
NP_000279.1:p.Gln301His
|
|