ENST00000319004.6:c.2583G>C
MANE Select
|
ENSP00000321706.5:p.Met861Ile
|
|
ENST00000319004.5:c.2583G>C
|
ENSP00000321706.5:p.Met861Ile
|
|
ENST00000576778.1:c.2550G>C
|
ENSP00000459565.1:p.Met850Ile
|
|
NM_015721.2:c.2583G>C
|
NP_056536.2:p.Met861Ile
|
|
XM_005256667.3:c.2595G>C
|
XP_005256724.1:p.Met865Ile
|
|
XM_005256668.3:c.2595G>C
|
XP_005256725.1:p.Met865Ile
|
|
XM_005256670.3:c.2550G>C
|
XP_005256727.1:p.Met850Ile
|
|
XM_011523910.1:c.2595G>C
|
XP_011522212.1:p.Met865Ile
|
|
XM_011523911.1:c.2595G>C
|
XP_011522213.1:p.Met865Ile
|
|
XM_011523912.1:c.2550G>C
|
XP_011522214.1:p.Met850Ile
|
|
XM_011523913.1:c.2550G>C
|
XP_011522215.1:p.Met850Ile
|
|
XM_005256667.4:c.2595G>C
|
XP_005256724.1:p.Met865Ile
|
|
XM_005256670.5:c.2550G>C
|
XP_005256727.1:p.Met850Ile
|
|
XM_011523910.2:c.2595G>C
|
XP_011522212.1:p.Met865Ile
|
|
XM_011523911.2:c.2595G>C
|
XP_011522213.1:p.Met865Ile
|
|
XM_011523912.2:c.2550G>C
|
XP_011522214.1:p.Met850Ile
|
|
XM_011523913.2:c.2550G>C
|
XP_011522215.1:p.Met850Ile
|
|
XM_017024709.1:c.2595G>C
|
XP_016880198.1:p.Met865Ile
|
|
NM_015721.3:c.2583G>C
MANE Select
|
NP_056536.2:p.Met861Ile
|
|