ENST00000336112.9:c.4217T>A
|
ENSP00000337250.5:p.Met1406Lys
|
|
ENST00000435504.9:c.4220T>A
MANE Select
|
ENSP00000391447.3:p.Met1407Lys
|
|
ENST00000336112.8:c.4136T>A
|
ENSP00000337250.4:p.Met1379Lys
|
|
ENST00000404843.5:c.2669T>A
|
ENSP00000383920.1:p.Met890Lys
|
|
ENST00000435504.8:c.4220T>A
|
ENSP00000391447.3:p.Met1407Lys
|
|
NM_018263.4:c.4220T>A
|
NP_060733.4:p.Met1407Lys
|
|
XM_006712039.2:c.3854T>A
|
XP_006712102.1:p.Met1285Lys
|
|
XM_006712040.1:c.3440T>A
|
XP_006712103.1:p.Met1147Lys
|
|
XM_011532950.1:c.4217T>A
|
XP_011531252.1:p.Met1406Lys
|
|
XM_011532951.1:c.4046T>A
|
XP_011531253.1:p.Met1349Lys
|
|
NM_018263.5:c.4220T>A
|
NP_060733.4:p.Met1407Lys
|
|
XM_006712039.3:c.3854T>A
|
XP_006712102.1:p.Met1285Lys
|
|
XM_006712040.2:c.3440T>A
|
XP_006712103.1:p.Met1147Lys
|
|
XM_011532950.3:c.4217T>A
|
XP_011531252.1:p.Met1406Lys
|
|
XM_011532951.2:c.4046T>A
|
XP_011531253.1:p.Met1349Lys
|
|
XM_017004430.1:c.3440T>A
|
XP_016859919.1:p.Met1147Lys
|
|
XM_024452974.1:c.4400T>A
|
XP_024308742.1:p.Met1467Lys
|
|
NM_001369346.1:c.4046T>A
|
NP_001356275.1:p.Met1349Lys
|
|
NM_001369347.1:c.3440T>A
|
NP_001356276.1:p.Met1147Lys
|
|
NM_018263.6:c.4220T>A
MANE Select
|
NP_060733.4:p.Met1407Lys
|
|