ENST00000374198.5:c.987G>A
MANE Select
|
ENSP00000363313.4:p.Met329Ile
|
|
ENST00000374199.9:c.990G>A
|
ENSP00000363315.4:p.Met330Ile
|
|
ENST00000374198.4:c.990G>A
|
ENSP00000363313.3:p.Met330Ile
|
|
ENST00000374199.8:c.987G>A
|
ENSP00000363315.3:p.Met329Ile
|
|
NM_001244926.1:c.987G>A
|
NP_001231855.1:p.Met329Ile
|
|
NM_004697.4:c.990G>A
|
NP_004688.2:p.Met330Ile
|
|
XM_005252300.2:c.261G>A
|
XP_005252357.1:p.Met87Ile
|
|
XM_011519181.1:c.990G>A
|
XP_011517483.1:p.Met330Ile
|
|
NM_001322266.1:c.261G>A
|
NP_001309195.1:p.Met87Ile
|
|
NM_001322267.1:c.261G>A
|
NP_001309196.1:p.Met87Ile
|
|
NR_136265.1:n.1100G>A
|
|
|
NR_136266.1:n.1097G>A
|
|
|
NM_001244926.2:c.987G>A
MANE Select
|
NP_001231855.1:p.Met329Ile
|
|
NM_001322266.2:c.261G>A
|
NP_001309195.1:p.Met87Ile
|
|
NM_001322267.2:c.261G>A
|
NP_001309196.1:p.Met87Ile
|
|
NM_004697.5:c.990G>A
|
NP_004688.2:p.Met330Ile
|
|
NR_136265.2:n.1076G>A
|
|
|
NR_136266.2:n.1073G>A
|
|
|