ENST00000399503.4:c.3155T>G
MANE Select
|
ENSP00000382423.3:p.Leu1052Trp
|
|
ENST00000399503.3:c.3155T>G
|
ENSP00000382423.3:p.Leu1052Trp
|
|
NM_005921.1:c.3155T>G
|
NP_005912.1:p.Leu1052Trp
|
|
XM_005248519.3:c.2777T>G
|
XP_005248576.2:p.Leu926Trp
|
|
XM_011543406.1:c.2900T>G
|
XP_011541708.1:p.Leu967Trp
|
|
XM_011543407.1:c.2876T>G
|
XP_011541709.1:p.Leu959Trp
|
|
XM_011543408.1:c.3155T>G
|
XP_011541710.1:p.Leu1052Trp
|
|
XM_017009484.1:c.2744T>G
|
XP_016864973.1:p.Leu915Trp
|
|
XM_017009485.1:c.2666T>G
|
XP_016864974.1:p.Leu889Trp
|
|
XR_001742068.2:n.3186T>G
|
|
|
NM_005921.2:c.3155T>G
MANE Select
|
NP_005912.1:p.Leu1052Trp
|
|