ENST00000267845.8:c.1872G>A
MANE Select
|
ENSP00000267845.3:p.Met624Ile
|
|
ENST00000267845.7:c.1872G>A
|
ENSP00000267845.3:p.Met624Ile
|
|
ENST00000543581.5:c.1773G>A
|
ENSP00000440252.1:p.Met591Ile
|
|
ENST00000559816.1:n.1616G>A
|
|
|
NM_001306146.1:c.1773G>A
|
NP_001293075.1:p.Met591Ile
|
|
NM_002112.3:c.1872G>A
|
NP_002103.2:p.Met624Ile
|
|
XM_011521479.1:c.1635G>A
|
XP_011519781.1:p.Met545Ile
|
|
XM_011521480.1:c.1440G>A
|
XP_011519782.1:p.Met480Ile
|
|
XM_017022094.1:c.1977G>A
|
XP_016877583.1:p.Met659Ile
|
|
XM_017022095.1:c.1878G>A
|
XP_016877584.1:p.Met626Ile
|
|
XM_017022096.1:c.1749G>A
|
XP_016877585.1:p.Met583Ile
|
|
XM_017022097.1:c.1740G>A
|
XP_016877586.1:p.Met580Ile
|
|
XM_017022098.1:c.1545G>A
|
XP_016877587.1:p.Met515Ile
|
|
NM_002112.4:c.1872G>A
MANE Select
|
NP_002103.2:p.Met624Ile
|
|
NM_001306146.2:c.1773G>A
|
NP_001293075.1:p.Met591Ile
|
|