ENST00000348729.8:c.914T>C
MANE Select
|
ENSP00000302701.4:p.Ile305Thr
|
|
ENST00000348729.7:c.914T>C
|
ENSP00000302701.4:p.Ile305Thr
|
|
ENST00000353963.7:c.926T>C
|
ENSP00000302851.5:p.Ile309Thr
|
|
ENST00000504513.1:c.164+267T>C
|
|
|
ENST00000506512.1:n.525T>C
|
|
|
NM_005847.4:c.914T>C
|
NP_005838.3:p.Ile305Thr
|
|
NM_152685.3:c.926T>C
|
NP_689898.2:p.Ile309Thr
|
|
XM_005272148.3:c.1034T>C
|
XP_005272205.3:p.Ile345Thr
|
|
XM_005272149.3:c.1022T>C
|
XP_005272206.3:p.Ile341Thr
|
|
XM_006714741.2:c.1034T>C
|
XP_006714804.2:p.Ile345Thr
|
|
XM_011543765.1:c.1034T>C
|
XP_011542067.1:p.Ile345Thr
|
|
XM_011543766.1:c.815T>C
|
XP_011542068.1:p.Ile272Thr
|
|
XM_011543767.1:c.719T>C
|
XP_011542069.1:p.Ile240Thr
|
|
XM_011543768.1:c.599T>C
|
XP_011542070.1:p.Ile200Thr
|
|
XM_011543769.1:c.209T>C
|
XP_011542071.1:p.Ile70Thr
|
|
XM_005272149.4:c.1022T>C
|
XP_005272206.3:p.Ile341Thr
|
|
XM_011543765.2:c.1034T>C
|
XP_011542067.1:p.Ile345Thr
|
|
NM_005847.5:c.914T>C
MANE Select
|
NP_005838.3:p.Ile305Thr
|
|
NM_152685.4:c.926T>C
|
NP_689898.2:p.Ile309Thr
|
|