ENST00000376199.7:c.903G>T
|
ENSP00000365372.2:p.Met301Ile
|
|
ENST00000376207.10:c.1008G>T
MANE Select
|
ENSP00000365380.4:p.Met336Ile
|
|
ENST00000455775.7:c.1077G>T
|
ENSP00000396415.3:p.Met359Ile
|
|
ENST00000518685.6:c.927G>T
|
ENSP00000428952.2:p.Met309Ile
|
|
ENST00000557224.6:c.903G>T
|
ENSP00000451208.1:p.Met301Ile
|
|
ENST00000651307.1:c.967+755G>T
|
ENSP00000498454.1:n.967+755G>T
|
|
ENST00000376197.1:c.858G>T
|
ENSP00000365369.1:p.Met286Ile
|
|
ENST00000376199.6:c.903G>T
|
ENSP00000365372.2:p.Met301Ile
|
|
ENST00000376207.8:c.1008G>T
|
ENSP00000365380.4:p.Met336Ile
|
|
ENST00000455775.6:c.1077G>T
|
ENSP00000396415.3:p.Met359Ile
|
|
ENST00000518685.5:c.903G>T
|
ENSP00000428952.1:p.Met301Ile
|
|
ENST00000557224.5:c.903G>T
|
ENSP00000451208.1:p.Met301Ile
|
|
NM_001114377.1:c.903G>T
|
NP_001107849.1:p.Met301Ile
|
|
NM_014009.3:c.1008G>T , LRG_62t1:c.1008G>T
|
NP_054728.2:p.Met336Ile
|
|
XM_006724533.2:c.1077G>T
|
XP_006724596.2:p.Met359Ile
|
|
XM_011543915.1:c.1227G>T
|
XP_011542217.1:p.Met409Ile
|
|
XM_011543916.1:c.1227G>T
|
XP_011542218.1:p.Met409Ile
|
|
XM_011543917.1:c.1026G>T
|
XP_011542219.1:p.Met342Ile
|
|
XM_011543918.1:c.1263G>T
|
XP_011542220.1:p.Met421Ile
|
|
XM_011543919.1:c.1227G>T
|
XP_011542221.1:p.Met409Ile
|
|
XM_017029567.1:c.954G>T
|
XP_016885056.1:p.Met318Ile
|
|
NM_001114377.2:c.903G>T
|
NP_001107849.1:p.Met301Ile
|
|
NM_014009.4:c.1008G>T
MANE Select
|
NP_054728.2:p.Met336Ile
|
|