ENST00000269228.10:c.3811G>C
MANE Select
|
ENSP00000269228.4:p.Glu1271Gln
|
|
ENST00000269228.9:c.3811G>C
|
ENSP00000269228.4:p.Glu1271Gln
|
|
ENST00000586150.5:c.509+1127G>C
|
|
|
ENST00000588867.1:n.1494G>C
|
|
|
ENST00000590723.5:c.163+1127G>C
|
ENSP00000464755.1:n.163+1127G>C
|
|
ENST00000591051.1:c.2889G>C
|
|
|
ENST00000591107.6:c.431+1127G>C
|
|
|
ENST00000593280.2:c.86+1127G>C
|
|
|
NM_000271.4:c.3811G>C
|
NP_000262.2:p.Glu1271Gln
|
|
XM_005258277.1:c.3805+1127G>C
|
XP_005258334.1:n.3805+1127G>C
|
|
XM_005258278.3:c.3862G>C
|
XP_005258335.1:p.Glu1288Gln
|
|
XM_005258279.1:c.3754+1127G>C
|
XP_005258336.1:n.3754+1127G>C
|
|
XM_006722479.2:c.3805+1127G>C
|
XP_006722542.1:n.3805+1127G>C
|
|
XM_011526015.1:c.3340+1127G>C
|
XP_011524317.1:n.3340+1127G>C
|
|
XM_005258278.5:c.3862G>C
|
XP_005258335.1:p.Glu1288Gln
|
|
XM_005258279.2:c.3754+1127G>C
|
XP_005258336.1:n.3754+1127G>C
|
|
XM_006722479.3:c.3805+1127G>C
|
XP_006722542.1:n.3805+1127G>C
|
|
XM_017025784.1:c.3805+1127G>C
|
XP_016881273.1:n.3805+1127G>C
|
|
XM_017025785.1:c.3805+1127G>C
|
XP_016881274.1:n.3805+1127G>C
|
|
XM_017025786.1:c.3754+1127G>C
|
XP_016881275.1:n.3754+1127G>C
|
|
XM_017025787.1:c.3754+1127G>C
|
XP_016881276.1:n.3754+1127G>C
|
|
NM_000271.5:c.3811G>C
MANE Select
|
NP_000262.2:p.Glu1271Gln
|
|