ENST00000399503.4:c.688G>T
MANE Select
|
ENSP00000382423.3:p.Ala230Ser
|
|
ENST00000399503.3:c.688G>T
|
ENSP00000382423.3:p.Ala230Ser
|
|
NM_005921.1:c.688G>T
|
NP_005912.1:p.Ala230Ser
|
|
XM_005248519.3:c.310G>T
|
XP_005248576.2:p.Ala104Ser
|
|
XM_011543406.1:c.433G>T
|
XP_011541708.1:p.Ala145Ser
|
|
XM_011543407.1:c.688G>T
|
XP_011541709.1:p.Ala230Ser
|
|
XM_011543408.1:c.688G>T
|
XP_011541710.1:p.Ala230Ser
|
|
XM_017009484.1:c.277G>T
|
XP_016864973.1:p.Ala93Ser
|
|
XM_017009485.1:c.199G>T
|
XP_016864974.1:p.Ala67Ser
|
|
XR_001742068.2:n.719G>T
|
|
|
NM_005921.2:c.688G>T
MANE Select
|
NP_005912.1:p.Ala230Ser
|
|