ENST00000399503.4:c.2556G>A
MANE Select
|
ENSP00000382423.3:p.Met852Ile
|
|
ENST00000399503.3:c.2556G>A
|
ENSP00000382423.3:p.Met852Ile
|
|
NM_005921.1:c.2556G>A
|
NP_005912.1:p.Met852Ile
|
|
XM_005248519.3:c.2178G>A
|
XP_005248576.2:p.Met726Ile
|
|
XM_011543406.1:c.2301G>A
|
XP_011541708.1:p.Met767Ile
|
|
XM_011543407.1:c.2277G>A
|
XP_011541709.1:p.Met759Ile
|
|
XM_011543408.1:c.2556G>A
|
XP_011541710.1:p.Met852Ile
|
|
XM_017009484.1:c.2145G>A
|
XP_016864973.1:p.Met715Ile
|
|
XM_017009485.1:c.2067G>A
|
XP_016864974.1:p.Met689Ile
|
|
XR_001742068.2:n.2587G>A
|
|
|
NM_005921.2:c.2556G>A
MANE Select
|
NP_005912.1:p.Met852Ile
|
|