ENST00000348729.8:c.827T>C
MANE Select
|
ENSP00000302701.4:p.Val276Ala
|
|
ENST00000348729.7:c.827T>C
|
ENSP00000302701.4:p.Val276Ala
|
|
ENST00000353963.7:c.839T>C
|
ENSP00000302851.5:p.Val280Ala
|
|
ENST00000504513.1:c.164+180T>C
|
|
|
ENST00000506512.1:n.438T>C
|
|
|
NM_005847.4:c.827T>C
|
NP_005838.3:p.Val276Ala
|
|
NM_152685.3:c.839T>C
|
NP_689898.2:p.Val280Ala
|
|
XM_005272148.3:c.947T>C
|
XP_005272205.3:p.Val316Ala
|
|
XM_005272149.3:c.935T>C
|
XP_005272206.3:p.Val312Ala
|
|
XM_006714741.2:c.947T>C
|
XP_006714804.2:p.Val316Ala
|
|
XM_011543765.1:c.947T>C
|
XP_011542067.1:p.Val316Ala
|
|
XM_011543766.1:c.728T>C
|
XP_011542068.1:p.Val243Ala
|
|
XM_011543767.1:c.632T>C
|
XP_011542069.1:p.Val211Ala
|
|
XM_011543768.1:c.512T>C
|
XP_011542070.1:p.Val171Ala
|
|
XM_011543769.1:c.122T>C
|
XP_011542071.1:p.Val41Ala
|
|
XM_005272149.4:c.935T>C
|
XP_005272206.3:p.Val312Ala
|
|
XM_011543765.2:c.947T>C
|
XP_011542067.1:p.Val316Ala
|
|
NM_005847.5:c.827T>C
MANE Select
|
NP_005838.3:p.Val276Ala
|
|
NM_152685.4:c.839T>C
|
NP_689898.2:p.Val280Ala
|
|