ENST00000399503.4:c.2716G>A
MANE Select
|
ENSP00000382423.3:p.Val906Ile
|
|
ENST00000399503.3:c.2716G>A
|
ENSP00000382423.3:p.Val906Ile
|
|
NM_005921.1:c.2716G>A
|
NP_005912.1:p.Val906Ile
|
|
XM_005248519.3:c.2338G>A
|
XP_005248576.2:p.Val780Ile
|
|
XM_011543406.1:c.2461G>A
|
XP_011541708.1:p.Val821Ile
|
|
XM_011543407.1:c.2437G>A
|
XP_011541709.1:p.Val813Ile
|
|
XM_011543408.1:c.2716G>A
|
XP_011541710.1:p.Val906Ile
|
|
XM_017009484.1:c.2305G>A
|
XP_016864973.1:p.Val769Ile
|
|
XM_017009485.1:c.2227G>A
|
XP_016864974.1:p.Val743Ile
|
|
XR_001742068.2:n.2747G>A
|
|
|
NM_005921.2:c.2716G>A
MANE Select
|
NP_005912.1:p.Val906Ile
|
|