ENST00000399503.4:c.3025T>A
MANE Select
|
ENSP00000382423.3:p.Phe1009Ile
|
|
ENST00000399503.3:c.3025T>A
|
ENSP00000382423.3:p.Phe1009Ile
|
|
NM_005921.1:c.3025T>A
|
NP_005912.1:p.Phe1009Ile
|
|
XM_005248519.3:c.2647T>A
|
XP_005248576.2:p.Phe883Ile
|
|
XM_011543406.1:c.2770T>A
|
XP_011541708.1:p.Phe924Ile
|
|
XM_011543407.1:c.2746T>A
|
XP_011541709.1:p.Phe916Ile
|
|
XM_011543408.1:c.3025T>A
|
XP_011541710.1:p.Phe1009Ile
|
|
XM_017009484.1:c.2614T>A
|
XP_016864973.1:p.Phe872Ile
|
|
XM_017009485.1:c.2536T>A
|
XP_016864974.1:p.Phe846Ile
|
|
XR_001742068.2:n.3056T>A
|
|
|
NM_005921.2:c.3025T>A
MANE Select
|
NP_005912.1:p.Phe1009Ile
|
|