ENST00000272286.4:c.1674G>A
MANE Select
|
ENSP00000272286.2:p.Met558Ile
|
|
ENST00000272286.2:c.1674G>A
|
ENSP00000272286.2:p.Met558Ile
|
|
NM_022437.2:c.1674G>A
|
NP_071882.1:p.Met558Ile
|
|
XM_005264483.2:c.1671G>A
|
XP_005264540.1:p.Met557Ile
|
|
XM_011533029.1:c.1686G>A
|
XP_011531331.1:p.Met562Ile
|
|
XM_011533030.1:c.1683G>A
|
XP_011531332.1:p.Met561Ile
|
|
XM_011533031.1:c.1458G>A
|
XP_011531333.1:p.Met486Ile
|
|
XR_939707.1:n.2176G>A
|
|
|
NM_001357321.1:c.1671G>A
|
NP_001344250.1:p.Met557Ile
|
|
XM_011533029.2:c.1686G>A
|
XP_011531331.1:p.Met562Ile
|
|
XM_011533030.2:c.1683G>A
|
XP_011531332.1:p.Met561Ile
|
|
XR_001738891.1:n.2190G>A
|
|
|
XR_939707.2:n.2190G>A
|
|
|
NM_022437.3:c.1674G>A
MANE Select
|
NP_071882.1:p.Met558Ile
|
|
NM_001357321.2:c.1671G>A
|
NP_001344250.1:p.Met557Ile
|
|